Devices and methods for molecule detection based on thermal stabilities of magnetic nanoparticles

ABSTRACT

Disclosed herein are detection methods that use magnetic nanoparticles (MNPs) to allow molecules to be identified. Embodiments of this disclosure include methods of using magnetic sensors (e.g., magnetoresistive sensors) to detect temperature-dependent magnetic fields (or changes in magnetic fields) emitted by MNPs, and, specifically to distinguish between the presence and absence of magnetic fields emitted, or not emitted, by MNPs at different temperatures selected to take advantage of knowledge of how the MNPs&#39; magnetic properties change with temperature. Embodiments disclosed herein may be used for nucleic acid sequencing, such as deoxyribonucleic acid (DNA) sequencing.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No.16/727,064, filed Dec. 26, 2019 and entitled “DEVICES AND METHODS FORMOLECULE DETECTION BASED ON THERMAL STABILITIES OF MAGNETICNANOPARTICLES” (Attorney Docket No. WDA-4279-US), which claims thebenefit of U.S. Provisional Application No. 62/833,206, filed Apr. 12,2019 and entitled “MAGNETORESISTIVE SENSOR ELEMENTS FOR NUCLEIC ACIDSEQUENCING ARRAYS AND DETECTION SCHEMES FOR NUCLEIC ACID SEQUENCINGUSING MAGNETIC NANOPARTICLES WITH DIFFERENT THERMAL STABILITY.” Both ofthe above-referenced applications are hereby incorporated by referencein their entireties for all purposes.

BACKGROUND Field of the Disclosure

Embodiments of the present disclosure generally relate to devices andmethods for using a magnetoresistive (MR) sensor array for moleculedetection, such as for nucleic acid sequencing (e.g., deoxyribonucleicacid (DNA) sequencing).

Description of the Related Art

Current state-of-the-art sequencing systems are based on fluorescencesignal detection and provide throughputs of 20 billion reads per run(www.illumina.com/systems/sequencing-platforms/novaseq.html). Achievingsuch performance, however, can require large-area flow cells,high-precision free-space imaging optics, and expensive high-powerlasers to generate sufficient fluorescence signals for successful basedetection.

One type of nucleic acid sequencing used for DNA sequencing is known as“sequencing by synthesis” (SBS). SBS involves binding ofprimer-hybridized template DNA, incorporation of a deoxynucleosidetriphosphate (dNTP), and detection of incorporated dNTP. Gradualincreases in SBS throughput have been accomplished in two ways, thefirst being an outward scaling, where the size and the number of flowcells in the sequencers is increased. This approach increases both thecost of reagents and the price of the sequencing system, as morehigh-power lasers and high-precision nano-positioners must be employed.The second approach involves inward scaling, where the density of DNAtesting sites is increased so that the total number of sequenced DNAstrands in a fixed-size flow cell is higher. To accomplish inwardscaling, increasingly higher numerical aperture (NA) lenses must beemployed to distinguish the signal from neighboring fluorophores as thespacing between them decreases. However, this approach cannot beimplemented indefinitely, as the Rayleigh criterion puts the distancebetween resolvable light point sources at 0.61λ/NA, constraining theminimum distance between two sequenced DNA strands to be no smaller thanapproximately 400 nm. Similar resolution limits apply to sequencingdirectly on top of imaging arrays (similar to cell phone cameras), wherethe smallest pixel size achieved so far is approximately 1 μm(www.ephotozine.com/article/complete-guide-to-image-sensor-pixel-size-29652).

The Rayleigh criterion currently represents the fundamental limitationfor inward scaling of optical SBS systems, which can only be overcome byapplying super-resolution imaging techniques (see A. M. Sydor, K. J.Czymmek, E. M. Puchner, and V. Mannella, “Super-Resolution Microscopy:From Single Molecules to Supramolecular Assemblies,” Special Issue:Quantitative Cell Biology, Vol. 25, 730, 2015) and has not yet beenachieved in highly multiplexed systems. Hence, increasing throughput anddecreasing cost of optical SBS sequencers has been slow due to the needto build bigger flow cells and implement more expensive optical scanningand imaging systems.

Therefore, there is a need for new and improved apparatuses for andmethods of detecting the presence of molecules such as nucleic acidsthat overcome the limitations of conventional apparatuses and methods.

SUMMARY

This summary represents non-limiting embodiments of the disclosure.

Disclosed herein are detection devices, systems, and methods that usemagnetic nanoparticles (MNPs) to allow molecules labeled by MNPs to bedetected. Embodiments of this disclosure are directed to variousdetection device and system embodiments using magnetic sensors capableof providing outputs indicating the presence or absence of MNPs near themagnetic sensors, and detection method embodiments designed to determine(e.g., measure or obtain) magnetic sensor outputs (e.g., a resistance, avoltage, a current, a frequency, a noise, or a change in resistance,voltage, current, frequency, or noise) indicative of the presence ofMNPs. Embodiments of the present disclosure generally relate to devicesand methods for using a magnetoresistive (MR) sensor array to detectmolecules. Embodiments disclosed herein may be used for nucleic acidsequencing, such as deoxyribonucleic acid (DNA) sequencing.

In some embodiments, a method of detecting molecules using a sequencingdevice comprising at least one fluidic channel and a plurality ofmagnetic sensors configured to detect MNPs within the fluidic channelcomprises, in one or more rounds of addition, adding, to the at leastone fluidic channel, first and second pluralities of molecules to bedetected. At least some of the first plurality of molecules to bedetected have been labeled by a first type of MNP, wherein, in a firsttemperature range, a magnitude of a magnetic field generated by thefirst type of MNP is greater than or equal to a first threshold, and, ina second temperature range, the magnitude of magnetic field generated bythe first type of MNP is less than the first threshold, wherein thefirst temperature range is lower than the second temperature range. Atleast some of the second plurality of molecules to be detected have beenlabeled by a second type of MNP, wherein, in the first and secondtemperature ranges, a magnitude of a magnetic field generated by thesecond type of MNP is greater than or equal to a second threshold, whichmay be the same as or different from the first threshold. The methodfurther comprises setting a temperature within the fluidic channel to bewithin the first temperature range, and obtaining an output from aselected one of the plurality of magnetic sensors while the temperatureof the fluidic channel is within the first temperature range, the outputindicating a magnitude of a first detected magnetic field. The methodfurther comprises setting the temperature within the fluidic channel tobe within the second temperature range, and obtaining the output fromthe selected one of the plurality of magnetic sensors while thetemperature of the fluidic channel is within the second temperaturerange, the output indicating a magnitude of a second detected magneticfield. The method further comprises determining, based at least in parton the magnitude of the first detected magnetic field and the magnitudeof the second detected magnetic field, whether the first type of MNP orthe second type of MNP has been detected by the selected one of theplurality of magnetic sensors.

In some embodiments, the output comprises one or more of a resistance, avoltage, a current, a frequency, a noise, or a change in resistance,voltage, current, frequency, or noise.

In some embodiments, determining whether the first type of MNP or thesecond type of MNP has been detected by the selected one of theplurality of magnetic sensors comprises (a) in response to the magnitudeof the first detected magnetic field being greater than or equal to thefirst threshold and the magnitude of the second detected magnetic fieldbeing less than the first threshold, determining that the first type ofMNP has been detected by the selected one of the plurality of magneticsensors, or (b) in response to the magnitude of the first detectedmagnetic field being greater than or equal to the second threshold andthe magnitude of the second detected magnetic field being greater thanor equal to the second threshold, determining that the second type ofMNP has been detected by the selected one of the plurality of magneticsensors.

In some embodiments, a Curie temperature of the first type of MNPdiffers from a Curie temperature of the second type of MNP. In some suchembodiments, the Curie temperature of the second type of MNP is greaterthan the Curie temperature of the first type of MNP, and the methodfurther comprises setting the temperature within the fluidic channel toa temperature value higher than the Curie temperatures of the first andsecond types of MNP before adding the first and second pluralities ofmolecules to be detected to the fluidic channel, and adding the firstand second pluralities of molecules to be detected to the fluidicchannel occurs while the temperature within the fluidic channel is atthe temperature value higher than the Curie temperatures of the firstand second types of MNP. In some embodiments in which the Curietemperature of the first type of MNP differs from the Curie temperatureof the second type of MNP, the method further comprises setting atemperature of a mixture of the first and second pluralities ofmolecules to be detected to a temperature value higher than the Curietemperatures of the first and second types of MNP before adding thefirst and second pluralities of molecules to be detected to the fluidicchannel.

In some embodiments, a blocking temperature of the first type of MNPdiffers from a blocking temperature of the second type of MNP.

In some embodiments, each of the first and second types of MNP ischaracterized by a blocking temperature, and the method furthercomprises setting the temperature within the fluidic channel to atemperature value higher than both of the blocking temperatures of thefirst and second types of MNP before adding the first and secondpluralities of molecules to be detected to the fluidic channel, andadding the first and second pluralities of molecules to be detected tothe fluidic channel occurs while the temperature within the fluidicchannel is at the temperature value higher than the blockingtemperatures of the first and second types of MNP. In some embodiments,each of the first and second types of MNP is characterized by a blockingtemperature, and the method further comprises setting a temperature of amixture of the first and second pluralities of molecules to be detectedto a temperature value higher than both of the blocking temperatures ofthe first and second types of MNP before adding the first and secondpluralities of molecules to be detected to the fluidic channel.

In some embodiments, first, second, and third pluralities of moleculesare added to the fluidic channel. In some such embodiments, themagnitude of the magnetic field generated by the first type of MNP isless than the first threshold in a third temperature range, the thirdtemperature range being higher than the second temperature range, andthe magnitude of the magnetic field generated by the second type of MNPis less than the second threshold in the third temperature range. Insome such embodiments, the method further comprises adding a thirdplurality of molecules to be detected to the fluidic channel, at leastsome of the third plurality of molecules to be detected being labeled bya third type of MNP, wherein, in the first, second, and thirdtemperature ranges, a magnitude of a magnetic field generated by thethird type of MNP is greater than or equal to a third threshold; settingthe temperature within the fluidic channel to be within the thirdtemperature range; obtaining the output of the selected one of theplurality of magnetic sensors while the temperature of the fluidicchannel is within the third temperature range, the output indicating amagnitude of a third detected magnetic field; and determining, based atleast in part on the magnitude of the third detected magnetic field,whether the third type of MNP has been detected by the selected one ofthe plurality of magnetic sensors. In some such embodiments,determining, based at least in part on the magnitude of the thirddetected magnetic field, whether the third type of MNP has been detectedby the selected one of the plurality of magnetic sensors comprises, inresponse to the magnitude of the first detected magnetic field beinggreater than or equal to the third threshold, and the magnitude of thesecond detected magnetic field being greater than or equal to the thirdthreshold, and the magnitude of the third detected magnetic field beinggreater than or equal to the third threshold, determining that the thirdtype of MNP has been detected by the selected one of the plurality ofmagnetic sensors. In some embodiments, at least two of the first,second, and third thresholds are different.

In some embodiments in which first, second, and third pluralities ofmolecules are added to the fluidic channel, the first, second, and thirdpluralities of molecules are added to the fluidic channel at asubstantially same time.

In some embodiments in which first, second, and third pluralities ofmolecules are added to the fluidic channel, a Curie temperature of thethird type of MNP is higher than a Curie temperature of the second typeof MNP, and the Curie temperature of the second type of MNP is higherthan a Curie temperature of the first type of MNP.

In some embodiments in which first, second, and third pluralities ofmolecules are added to the fluidic channel, the method further comprisessetting the temperature within the fluidic channel to a temperaturevalue higher than the Curie temperatures of the first, second, and thirdtypes of MNP before adding the first, second, and third pluralities ofmolecules to be detected to the fluidic channel, and adding the first,second, and third pluralities of molecules to be detected to the fluidicchannel occurs while the temperature within the fluidic channel is atthe temperature value higher than the Curie temperatures of the first,second, and third types of MNP.

In some embodiments in which first, second, and third pluralities ofmolecules are added to the fluidic channel, a blocking temperature ofthe third type of MNP differs from a blocking temperature of the secondtype of MNP, and the blocking temperature of the second type of MNPdiffers from a blocking temperature of the first type of MNP.

In some embodiments, first, second, third, and fourth pluralities ofmolecules are added to the fluidic channel. In some such embodiments,the magnitude of the magnetic field generated by the first type of MNPis less than the first threshold in a fourth temperature range, thefourth temperature range being higher than the third temperature range,the magnitude of the magnetic field generated by the second type of MNPis less than the second threshold in the fourth temperature range, andthe magnitude of the magnetic field generated by the third type of MNPis less than the third threshold in the fourth temperature range. Insome such embodiments, the method further comprises adding a fourthplurality of molecules to be detected to the fluidic channel, at leastsome of the fourth plurality of molecules to be detected being labeledby a fourth type of MNP, wherein, in the first, second, third, andfourth temperature ranges, a magnitude of a magnetic field generated bythe fourth type of MNP is greater than or equal to a fourth threshold;setting the temperature within the fluidic channel to be within thefourth temperature range; obtaining the output of the selected one ofthe plurality of magnetic sensors while the temperature of the fluidicchannel is within the fourth temperature range, the output indicating amagnitude of a fourth detected magnetic field; and determining, based atleast in part on the magnitude of the fourth detected magnetic field,whether the fourth type of MNP has been detected by the selected one ofthe plurality of magnetic sensors.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, determiningwhether the fourth type of MNP has been detected by the selected one ofthe plurality of magnetic sensors comprises, in response to themagnitude of the first detected magnetic field being greater than orequal to the fourth threshold, and the magnitude of the second detectedmagnetic field being greater than or equal to the fourth threshold, andthe magnitude of the third detected magnetic field being greater than orequal to the fourth threshold, and the magnitude of the fourth detectedmagnetic field being greater than or equal to the fourth threshold,determining that the fourth type of MNP has been detected by theselected one of the plurality of magnetic sensors. In some suchembodiments, two or more of the first, second, third, and fourththresholds are different.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, the first,second, third, and fourth plurality of molecules to be detected areadded to the fluidic channel at a substantially same time.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, a Curietemperature of the fourth type of MNP is higher than a Curie temperatureof the third type of MNP, the Curie temperature of the third type of MNPis higher than a Curie temperature of the second type of MNP, and theCurie temperature of the second type of MNP is higher than a Curietemperature of the first type of MNP.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, the methodfurther comprises setting the temperature within the fluidic channel toa temperature value higher than the Curie temperatures of the first,second, third, and fourth types of MNP before adding the first, second,third, and fourth pluralities of molecules to be detected to the fluidicchannel, and adding the first, second, third, and fourth pluralities ofmolecules to be detected to the fluidic channel occurs while thetemperature within the fluidic channel is at the temperature valuehigher than the Curie temperatures of the first, second, third, andfourth types of MNP.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, a blockingtemperature of the fourth type of MNP differs from a blockingtemperature of the third type of MNP, the blocking temperature of thethird type of MNP differs from a blocking temperature of the second typeof MNP, and the blocking temperature of the second type of MNP differsfrom a blocking temperature of the first type of MNP.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, the magnitudeof the magnetic field generated by the first type of MNP is less thanthe first threshold in a fourth temperature range, the fourthtemperature range being higher than the third temperature range, themagnitude of the magnetic field generated by the second type of MNP isless than the second threshold in the fourth temperature range, and themagnitude of the magnetic field generated by the third type of MNP isless than the third threshold in the fourth temperature range. In somesuch embodiments, the method further comprises adding a fourth,unlabeled plurality of molecules to be detected to the fluidic channel,setting the temperature within the fluidic channel to be within thefourth temperature range, obtaining the output of the selected one ofthe plurality of magnetic sensors while the temperature of the fluidicchannel is within the fourth temperature range, the output indicating amagnitude of a fourth detected magnetic field, and, in response to themagnitude of the fourth detected magnetic field being less than thefirst threshold, less than the second threshold, and less than the thirdthreshold, determining that none of the first, second, or third types ofMNP has been detected by the selected one of the plurality of magneticsensors.

In some embodiments in which first, second, third, and fourthpluralities of molecules are added to the fluidic channel, the magnitudeof the magnetic field generated by the first type of MNP is less thanthe first threshold in a fourth temperature range, the fourthtemperature range being higher than the third temperature range, themagnitude of the magnetic field generated by the second type of MNP isless than the second threshold in the fourth temperature range, and themagnitude of the magnetic field generated by the third type of MNP isless than the third threshold in the fourth temperature range. In somesuch embodiments, the method further comprises adding, to the fluidicchannel, a fourth, unlabeled plurality of molecules to be detected,setting the temperature within the fluidic channel to be within thefourth temperature range, obtaining the output of the selected one ofthe plurality of magnetic sensors while the temperature of the fluidicchannel is within the fourth temperature range, the output indicating amagnitude of a fourth detected magnetic field, and in response to themagnitude of the fourth detected magnetic field being less than thefirst threshold, less than the second threshold, and less than the thirdthreshold, determining that one of the fourth, unlabeled plurality ofmolecules has been detected by the selected on of the plurality ofmagnetic sensors.

In some embodiments, a system for sequencing nucleic acid comprises (a)a fluidic channel having a plurality of sites for attaching, to asurface of the fluidic channel, a plurality of nucleic acid strands tobe sequenced, (b) a temperature control device coupled to the fluidicchannel for setting a temperature of a contents of the fluidic channelto be within any of first, second, and third temperature ranges, whereinthe first, second, and third temperature ranges are nonoverlapping, (c)a plurality of magnetic sensors configured to detect a magnetic fieldemitted by one or more magnetic nanoparticles (MNPs) at each of theplurality of sites in each of the first, second, and third temperatureranges, and (d) at least one processor coupled to the magnetic sensorsand to the temperature control device and configured to execute at leastone machine-executable instruction. In some embodiments, at least one ofthe plurality of magnetic sensors comprises a magnetoresistive (MR)sensor. In some embodiments, the at least one machine-executableinstruction, when executed, causes the at least one processor to (i)direct the temperature control device to set the temperature of thecontents of the fluidic channel to be within the first temperaturerange, (ii) obtain a first output from a magnetic sensor associated witha particular site of the plurality of sites, the first output indicatinga magnitude of a first detected magnetic field, (iii) direct thetemperature control device to set the temperature of the contents of thefluidic channel to be within the second temperature range, (iv) obtain asecond output of the magnetic sensor associated with the particular siteof the plurality of sites, the second output indicating a magnitude of asecond detected magnetic field, (v) direct the temperature controldevice to set the temperature of the contents of the fluidic channel tobe within the third temperature range, (vi) obtain a third output of themagnetic sensor associated with the particular site of the plurality ofsites, the third output indicating a magnitude of a third detectedmagnetic field, and (vii) determine, based at least in part on themagnitude of the first detected magnetic field, the magnitude of thesecond detected magnetic field, and the magnitude of the third detectedmagnetic field, whether a MNP of a particular type has been detected bythe magnetic sensor. In some embodiments, at least one of the first,second, or third outputs comprises one or more of a resistance, avoltage, a current, a frequency, a noise, or a change in resistance,voltage, current, frequency, or noise. In some embodiments, the firsttemperature range is lower than the second temperature range, and thesecond temperature range is lower than the third temperature range.

In some embodiments, the fluidic channel comprises a structurecomprising the plurality of sites for attaching, to the surface of thefluidic channel, the plurality of nucleic acid strands to be sequenced.In some such embodiments, the structure comprises a cavity or a ridge.

In some embodiments, the at least one machine-executable instruction,when executed, causes the at least one processor to determine whether aMNP of a particular type has been detected by the magnetic sensor by oneor more of: (a) in response to the magnitude of the first detectedmagnetic field meeting or exceeding a first threshold, and the magnitudeof the second detected magnetic field not meeting the first threshold,and the magnitude of the third detected magnetic field not meeting thefirst threshold, determining that a MNP of a first type has beendetected by the magnetic sensor, (b) in response to the magnitude of thefirst detected magnetic field meeting or exceeding a second threshold,the magnitude of the second detected magnetic field meeting or exceedingthe second threshold, and the magnitude of the third detected magneticfield not meeting the second threshold, determining that a MNP of asecond type has been detected by the magnetic sensor, or (c) in responseto the magnitude of the first detected magnetic field meeting orexceeding a third threshold, and the magnitude of the second detectedmagnetic field meeting or exceeding the third threshold, and themagnitude of the third detected magnetic field meeting or exceeding thethird threshold, determining that a MNP of a third type has beendetected by the magnetic sensor.

In some embodiments, when executed by the at least one processor, the atleast one machine-executable instruction further causes the at least oneprocessor to (a) direct the temperature control device to set thetemperature of the contents of the fluidic channel to be within a fourthtemperature range, the fourth temperature range being higher than thethird temperature range, (b) obtain a fourth output from a magneticsensor associated with a particular site of the plurality of sites, thefourth output indicating a magnitude of a fourth detected magneticfield, and (c) in response to the magnitude of the first detectedmagnetic field meeting or exceeding a fourth threshold, and themagnitude of the second detected magnetic field meeting or exceeding thefourth threshold, and the magnitude of the third detected magnetic fieldmeeting or exceeding the fourth threshold, and the fourth detectedmagnetic field meeting or exceeding the fourth threshold, determiningthat a MNP of a fourth type has been detected by the magnetic sensor.

In some embodiments including a temperature control device, thetemperature control device comprises at least one of a thermal sensor ora microprocessor. In some embodiments including a temperature controldevice, the temperature control device comprises a heater.

In some embodiments, a system for detecting magnetic nanoparticles(MNPs) coupled to molecules, the MNPs being characterized by acharacteristic temperature below which the MNPs emit a magnetic fieldhaving a magnitude higher than a threshold and above which the MNPs donot emit the magnetic field having the magnitude higher than thethreshold, comprises (a) a fluidic channel, (b) a temperature controldevice coupled to the fluidic channel for setting a temperature of acontents of the fluidic channel, (c) control circuitry coupled to thetemperature control device and configured to direct the temperaturecontrol device to set the temperature of the contents of the fluidicchannel to a first temperature and to a second temperature, the firsttemperature being higher than the characteristic temperature of the MNPsand the second temperature being lower than the characteristictemperature of the MNPs, (d) a magnetic sensor configured to detect amagnetic field emitted by one or more MNPs in the fluidic channel, and(e) detection circuitry coupled to the magnetic sensor and configured toobtain, from the magnetic sensor, an output indicating a magnetic fieldmagnitude detected by the magnetic sensor.

In some embodiments, the characteristic temperature is a Curietemperature. In some embodiments, the characteristic temperature is ablocking temperature.

In some embodiments, the control circuitry is further configured todetermine, based at least in part on the magnetic field magnitudedetected by the magnetic sensor, whether a MNP has been detected by themagnetic sensor.

In some embodiments, the temperature of the contents of the fluidicchannel is less than the characteristic temperature, and the at leastone processor is configured to determine whether a MNP has been detectedby the magnetic sensor by (i) comparing the magnetic field magnitudedetected by the magnetic sensor to the threshold, and (ii) in responseto the magnetic field magnitude detected by the magnetic sensor beinggreater than the threshold, determining that the MNP has been detectedby the magnetic sensor.

In some embodiments, the temperature of the contents of the fluidicchannel is greater than the characteristic temperature, and the at leastone processor is configured to determine whether a MNP has been detectedby the magnetic sensor by (i) comparing the magnetic field magnitudedetected by the magnetic sensor to the threshold, and (ii) in responseto the magnetic field magnitude detected by the magnetic sensor beingless than the threshold, determining that the MNP has been detected bythe magnetic sensor.

In some embodiments, the fluidic channel comprises a structure, and thestructure comprises the plurality of sites for attaching, to the surfaceof the fluidic channel, a plurality of unidentified molecules to beidentified. In some such embodiments, the structure comprises a cavityor a ridge.

In some embodiments, the temperature control device comprises at leastone of a thermal sensor or a microprocessor. In some embodiments, thetemperature control device comprises a heater.

In some embodiments, the magnetic sensor comprises a magnetoresistive(MR) sensor. In some embodiments, the output comprises one or more of aresistance, a voltage, a current, a frequency, a noise, or a change inresistance, voltage, current, frequency, or noise.

BRIEF DESCRIPTION OF THE DRAWINGS

So that the manner in which the above-recited features of the presentdisclosure can be understood in detail, a more particular description ofthe disclosure is provided in reference to embodiments, some of whichare illustrated in the appended drawings. It is to be noted, however,that the appended drawings illustrate only typical embodiments of thisdisclosure and are therefore not to be considered limiting of its scope,for the disclosure may admit to other equally-effective embodiments.Objects, features, and advantages of the disclosure will be readilyapparent from the following description of certain embodiments taken inconjunction with the accompanying drawings in which:

FIG. 1 illustrates an exemplary MNP, suitable for use in accordance withsome embodiments, having a magnetization that is illustratively fixedalong the z-axis due to magnetic anisotropy.

FIG. 2A illustrates an exemplary sequential binary method suitable forDNA sequencing in accordance with some embodiments.

FIG. 2B illustrates an exemplary method suitable for DNA sequencing inaccordance with some embodiments.

FIGS. 3A through 3E illustrate sequencing operations using different MNPtypes for nucleic acid sequencing in accordance with some embodiments.

FIG. 4 illustrates another exemplary method suitable for DNA sequencingin accordance with some embodiments.

FIGS. 5A, 5B, and 5C illustrate the basic construction of amagnetoresistive (MR) device and how it can be used as a magnetic sensorin accordance with some embodiments.

FIG. 6 illustrates a portion of a magnetic sensor in accordance withsome embodiments.

FIGS. 7A and 7B illustrate the resistance of MR sensors suitable for usein accordance with some embodiments.

FIGS. 8A, 8B, and 8C illustrate a cross-point array architecture of MRsensor elements in accordance with some embodiments.

FIGS. 9A, 9B, and 9C illustrate an exemplary detection device inaccordance with some embodiments.

FIG. 9D is a block diagram showing an exemplary detection system formolecule detection in accordance with some embodiments.

FIG. 10 is an exploded view of exemplary heating elements suitable forincorporation in or use with a detection device in accordance with someembodiments.

FIG. 11 illustrates an array of heating elements that may be coupled,for example, to the bottom surface of a detection device in accordancewith some embodiments.

FIGS. 12A, 12B, 12C, and 12D illustrate portions of an exemplarydetection device in accordance with some embodiments.

FIG. 12E illustrates an exemplary approach for selecting magneticsensors in accordance with some embodiments.

FIG. 12F illustrates another exemplary magnetic sensor selectionapproach in accordance with some embodiments.

FIGS. 13A and 13B illustrate a magnetic sensor and detection using thatmagnetic sensor in accordance with some embodiments.

FIG. 14 illustrates a method of manufacturing a detection device inaccordance with some embodiments.

FIG. 15 illustrates the results of each step of the fabrication processof FIG. 14 in accordance with some embodiments.

To facilitate understanding, identical reference numerals have beenused, where possible, to designate identical elements that are common tothe figures. It is contemplated that elements disclosed in oneembodiment may be beneficially utilized on other embodiments withoutspecific recitation.

DETAILED DESCRIPTION

Disclosed herein are improved detection devices, systems, and methodsthat use magnetic nanoparticles (MNPs) to allow molecules to beidentified. Embodiments of this disclosure are directed to variousdetection device and system embodiments using magnetic sensors capableof detecting the presence or absence of MNPs near the magnetic sensors,and detection method embodiments designed to determine (e.g., measure orobtain) outputs (e.g., resistance or change in resistance) indicative ofthe presence of MNPs. Embodiments of the present disclosure generallyrelate to devices and methods for using a magnetoresistive (MR) sensorarray to detect molecules. For example, embodiments disclosed herein maybe used for nucleic acid sequencing, such as deoxyribonucleic acid (DNA)sequencing.

Specifically, embodiments of this disclosure include magnetic sensors(e.g., magnetoresistive sensors) that can be used to detecttemperature-dependent magnetic fields (or temperature-dependent changesin magnetic fields) emitted by MNPs, and, specifically to distinguishbetween the presence and absence of magnetic fields emitted, or notemitted, by MNPs at different temperatures selected to take advantage ofknowledge of the MNPs' Curie temperatures.

In the following description, reference is made to embodiments of thedisclosure. It should be understood, however, that the disclosure is notlimited to specific described embodiments. Instead, any combination ofthe following features and elements, whether related to differentembodiments or not, is contemplated to implement and practice thedisclosure. Furthermore, although embodiments of the disclosure mayachieve advantages over other possible solutions and/or over the priorart, whether or not a particular advantage is achieved by a givenembodiment is not limiting of the disclosure. Thus, the followingaspects, features, embodiments and advantages are merely illustrative.Likewise, reference to “the disclosure” shall not be construed as ageneralization of any inventive subject matter disclosed herein.

The terms “over,” “under,” “between,” “on,” and other similar terms asused herein refer to a relative position of one layer with respect toother layers. As such, for example, one layer disposed over or underanother layer may be directly in contact with the other layer or mayhave one or more intervening layers. Moreover, one layer disposedbetween layers may be directly in contact with the two layers or mayhave one or more intervening layers. In contrast, a first layer “on” asecond layer is in contact with the second layer. The relative positionof the terms does not define or limit the layers to a vector spaceorientation of the layers.

The term “coupled” is used herein to refer to elements that are eitherdirectly connected or connected through one or more interveningelements. For example, as explained below, a line (e.g., for selectingor reading an output from a magnetic sensor) may be directly connectedto a magnetic sensor, or it may be connected to the sensor viaintervening elements.

The terms “sense” and “detect” are used interchangeably herein to meanobtain information from a physical stimulus. Sensing and detectinginclude measuring.

Although some of the disclosure herein is provided in the context ofnucleic acid sequencing, and specifically DNA sequencing, it is to beunderstood that the embodiments herein generally may be used to detectany type of molecule to which a magnetic particle (e.g., a magneticnanoparticle) can be attached. The disclosure presumes that theparticles attached are magnetic nanoparticles, but this presumption isexemplary and is not intended to be limiting. Any molecule type that canbe labeled by a magnetic nanoparticle may be detected using the methodsand detection devices disclosed herein. Such molecule types may bebiologic molecule types, such as proteins, antibodies, etc. For example,the disclosures herein may be used to detect nucleic acids (e.g., in DNAsequencing). The disclosures herein may also be used to detectnon-biologic (inorganic or non-living) molecules, such as contaminants,minerals, chemical compounds, etc. The presentation of portions of thedisclosure in the context of nucleic acid sequencing is solely exemplaryand is not intended to limit the scope of the present disclosure.

Furthermore, although the description herein focuses on DNA as anexemplary nucleic acid, the various embodiments described can be appliedto nucleic acid sequencing in general. Similarly, although SBS is usedfor illustrative purposes in the following description, the variousembodiments are not so limited to SBS sequencing protocols (e.g.,dynamic sequencing could be used instead).

Conventional nucleic acid sequencing, such as that used for DNAsequencing, typically relies on the detection of fluorescence.Specifically, fluorescence-based technologies used to differentiatebetween different bases in a sample (e.g., in fluorescence-based nucleicacid sequencing technologies) rely on, for example, the quality of asignal generated by a detection moiety that is associated with aparticular type of nucleotide. For example, conventional fluorescentsequencing technologies utilize identifiably-distinct fluorescentmoieties, each attached to one of the four nucleotides A, T, C, and Gthat are utilized in a sequencing reaction.

One conventional method of DNA sequencing involves adaptingsingle-strand DNA (ssDNA) for attachment to a solid support of asequencing apparatus and amplifying the quantity of the ssDNA usingtechniques such as the polymerase chain reaction to create many DNAmolecules with a short leader. An oligo complementary to the shortleader may then be added so that there is a short section ofdouble-stranded DNA (dsDNA) at the leader. The double stranded portionof the bound molecule is a primer for a suitable DNA polymerase, suchas, for example, Taq polymerase, which is operable at high temperatures.

The sequencing can then take one of several approaches. For example, thesequencing can use a mixture of four fluorescently-labeled 3′-blockeddNTPs (fluorescently labeled dideoxynucleotide terminators), where thefluorescent label is part of the 3′-blocking group. The fluorescentlabel serves as a “reversible terminator” for polymerization. Each ofthe NTPs is labeled by a different label (i.e., each of the A, G, C, andT nucleotides has a different label), and the different labels aredistinguishable by fluorescent spectroscopy or by other optical means.

Four fluorescently-labeled nucleotide precursors can be used to sequencemillions of clusters of DNA strands in parallel. DNA polymerasecatalyzes the incorporation of fluorescently-labeled dNTPs into a DNAtemplate strand during sequential cycles of DNA synthesis. In eachsequencing cycle, the bound double strand DNA molecule is exposed to DNApolymerase and a mixture of the four fluorescently-labeled 3′-blockedNTPs. The polymerase adds one of the four dNTPs to the growingoligonucleotide chain (whichever dNTP is complementary to the nextunpaired base in the ssDNA). The unincorporated dNTPs and otherimpurities that are either left unreacted or generated during thereactions are then separated from the vicinity of the support-bound DNAby washing at a temperature that prevents the free dNTPs from binding tothe ssDNA but is not so high as to dehybridize the dsDNA.

Because only one of the four types of dNTP will have been added to theoligonucleotide, and the four fluorescent labels are distinguishable,the identity of the incorporated dNTP can be identified through laserexcitation and imaging. Specifically, each of four filters is used todetermine whether light of a particular wavelength (e.g., color) isemitted. The fluorescent label can then be enzymatically cleaved toallow the next round of incorporation. Because each base type can pairwith one and only one other base type, the identity of the just-pairedbase in the unknown sequence of the ssDNA is known from the identity ofthe incorporated dNTP (which is known from the wavelength of emittedlight). Thus, the base is identified directly from fluorescencemeasurements during each cycle.

One disadvantage of the above-described approach is that a complicatedoptics system is needed to filter out different wavelengths of light todetect the fluorescent labels of the incorporated dNTPs and todistinguish between the different emitted colors. Other approaches havebeen developed to simplify the optics system, but they are slower tosequence and require intermediate chemistry steps within each sequencingcycle. Thus, these approaches have been introduced in smaller, lessexpensive entry-level sequencing systems but not in higher-level systemsrequiring fast throughput.

Disclosed herein are improved detection devices, systems, and methodsthat use magnetic nanoparticles (MNPs) to allow molecules to beidentified. Embodiments of this disclosure are directed to variousdetection device and system embodiments using magnetic sensors capableof obtaining outputs indicating the presence or absence of MNPs near themagnetic sensors, and detection method embodiments designed to determine(e.g., measure or obtain) outputs (e.g., resistance or change inresistance) indicative of the presence of MNPs.

As explained previously, the disclosures herein may be used to detectany type of molecule (e.g., biologic, organic, inorganic, or non-living)to which a magnetic particle (e.g., a MNP) can be attached. Apparatusesand methods disclosed herein use MNPs and magnetic sensors to performdetection of molecules, such as in nucleic acid sequencing (e.g., DNAsequencing using SBS chemistry methods). Specifically, embodiments ofthis disclosure include magnetic sensors (e.g., magnetoresistivesensors) that can be used to detect temperature-dependent magneticfields (or changes in magnetic fields) emitted by MNPs, and,specifically to distinguish between the presence and absence of magneticfields emitted, or not emitted, by MNPs at different temperaturesselected to take advantage of knowledge of the MNPs' Curie temperatures.Embodiments that use the same MNP type for all molecules to be detectedare disclosed, as are embodiments that use multiple MNP types, each typelabeling a different molecule type and having a different Curietemperature. The disclosed embodiments allow different types of detectedmolecules to be distinguished. Moreover, by appropriate selection of theMNPs and their Curie temperatures, and the temperature at whichMNP-labeled molecules are added to a fluidic channel of a detectiondevice, clumping or clustering of MNP-labeled molecules added to adetection device can be mitigated.

Certain embodiments of the present disclosure also include variousdetection methods to obtain or determine (e.g., measure) outputs of themagnetic sensors (e.g., a resistance, a voltage, a current, a frequency,a noise, and/or a change in resistance, voltage, current, frequency,and/or noise) caused by MNPs used as labels being near the magneticsensors. Knowledge of which particular molecule type (e.g., in DNAsequencing applications, the type of base) to which the particular MNPlabel has been attached, and the Curie temperature of that molecule, maythen be used to identify the particular molecule type (e.g., in DNAsequencing applications, the last-paired base of the ssDNA strand).

MNPs

MNPs that are suitable for use in biologic molecule detectionapplications have a wide range of sizes (e.g., tens to hundreds ofnanometers (nm)) and shapes (e.g., spherical, cubic, pyramidal, etc.).The magnetism in these particles is due to exchange interactions in thematerials that align unpaired core electrons in the material's latticein the same direction, resulting in a net moment of angular momentum inthe material that is also called the magnetic moment or magnetization ofthe nanoparticle. (The terms “magnetic moment” and “magnetization” areused interchangeably herein.) The magnetic moment (a dipole momentwithin an atom that originates from the angular momentum and spin ofelectrons) of the MNP, at least at some temperatures, gives rise tomagnetic fields that, as described further below, can be used to detectthe presence of the MNP. Additional magnetic anisotropy energies (e.g.,magnetocrystalline, demagnetization) also help define stableorientations for the magnetization of the MNP, so that, when the spatialorientation of a particle is well defined, so is the magnetizationdirection of the particle. FIG. 1 illustrates an exemplary MNP having amagnetization that is illustratively fixed along the z-axis due tomagnetic anisotropy. It is to be understood that if the particle ismechanically rotated, so is the magnetization direction.

The magnetization of a MNP is temperature-dependent, and for MNPs thatare sufficiently small, there are two temperatures at which theirmagnetic properties change significantly. The first change occurs atwhat is referred to as the blocking temperature, denoted as T_(B). Whena nanoparticle is sufficiently small, its magnetization can flipdirection randomly in the absence of an external magnetic field. At thispoint, the thermal energy of the particle (kT) is sufficiently largerthan the anisotropy energies such that the magnetization no longerpoints along a single axis. Instead, the magnetization can randomly flipor rotate between two or more orientations, at which point the MNPtransitions from being ferromagnetic to being consideredsuperparamagnetic. (Magnetic nanoparticles are said to be“superparamagnetic” when the loop area of their hysteresis loop, whenmeasured under quasi-static conditions, is zero, which occurs when thenanoparticle cores are small enough to support only one magnetic domainper core, in which case they are single-domain particles.)

The magnetic properties of a MNP also change at or around the Curietemperature, denoted as T_(c), which is greater than or equal to theblocking temperature. The Curie temperature (sometimes referred to asthe ferromagnetic transition temperature) is the temperature above whichferromagnetic materials lose their permanent magnetic properties andbecome paramagnetic. Ferromagnetic and paramagnetic materials havedifferent intrinsic magnetic moment structures, and these propertieschange at a material's Curie temperature. Stated another way,ferromagnetism appears only below the Curie temperature. At temperaturesabove the Curie temperature, the thermal energies are large enough toovercome the exchange interactions amongst the core electrons andeliminate the net moment of the MNP. Consequently, the ordered magneticmoments change and become disordered (e.g., oriented randomly, resultingin a zero net magnetization). Below the Curie temperature, a MNP isferromagnetic (has moments that are magnetized spontaneously) and, assuch, generates a magnetic field, but above the Curie temperature, theparticle is in a paramagnetic state and does not generate a spontaneousmagnetic field of its own.

The inventors of the present disclosure had the insight that thedifferences in MNPs' magnetic properties around the blocking temperatureand around the Curie temperature can be exploited for moleculedetection, as explained in further detail below.

As will be appreciated by those having ordinary skill in the art, thereare many suitable MNPs that can be used with the systems and methodsdescribed below. For example, the Curie temperature of a MNP may beadjusted over a small range between room temperature and 100° C. bychanging the composition of compounds. For example, Y₃Fe_(5-x) Al_(x)O₁₂particles with an average diameter of 100 nm and with Curie temperaturesvarying from 7 to 140° C. by varying the aluminum content in the MNPhave been synthesized (see, e.g., Grasset et al., “Synthesis, magneticproperties, surface modification and cytotoxicity evaluation ofY₃Fe_(5-x)Al_(x)O₁₂ garnet submicron particles for biomedicalapplications,” JMMM, 234 (2001) 409-418, which is hereby incorporated byreference in its entirety for all purposes).La_(1-x)Sr_(x)Mn_(1-y)Ti_(y)O₃ particles having Curie temperaturesbetween 20 and 90° C. by varying the titanium content have also beensynthesized (see, e.g., Phuc et al., “Tuning of the Curie Temperature inLa_(1-x)Sr_(x)Mn_(1-y)Ti_(y)O₃,” Journal of the Korean Physical Society,Vol. 52, No. 5, May 2008, pp. 1492-1495, which is hereby incorporated byreference in its entirety for all purposes). Finally, GdSi alloys dopedwith elements such as germanium, erbium, and rhodium have shown Curietemperatures in a range around room temperature with smaller(approximately 40 nm diameter) sizes and more regular spherical shapes(see, e.g., Alnasir et. al, “Magnetic and magnetothermal studies of pureand doped gadolinium silicide nanoparticles for self-controlledhyperthermia applications,” JMMM, 449 (2018) 137-144, which is herebyincorporated by reference in its entirety for all purposes). Theseexamples represent only a small sample of possible materials forgenerating MNPs suitable for use with the disclosed embodiments and arenot meant to be limiting. Those having skill in the art will understandthat many MNPs having the properties described in this disclosure existor can be developed without substantial experimentation. Moreover, thoseskilled in the art will recognize that the blocking temperature may alsobe adjusted by doping, for example, by changing the crystallinestructure of a material.

Once the MNPs have been selected, there are a number of ways to attachthe MNPs to the molecules to be detected and (if applicable) to cleavethe MNPs following detection. For example, the MNPs may be attached to abase or a molecule to be detected, in which case the MNPs may be cleavedchemically. As another example, the MNPs may be attached to a phosphate,in which case the MNPs may be cleaved by, for example, polymerase or, ifattached via a linker, by cleaving the linker.

In some embodiments for nucleic acid sequencing, the MNP is linked tothe nitrogenous base (e.g., A, C, T, G, or a derivative) of thenucleotide precursor. After incorporation of the nucleotide precursorand detection by a detection device (e.g., as described below), the MNPmay be cleaved from the incorporated nucleotide.

In some embodiments, the MNP is attached via a cleavable linker.Cleavable linkers are known in the art and have been described, e.g., inU.S. Pat. Nos. 7,057,026, 7,414,116 and continuations and improvementsthereof. In some embodiments, the MNP is attached to the 5-position inpyrimidines or the 7-position in purines via a linker comprising anallyl or azido group. In some embodiments, the linker comprises adisulfide, indole, a Sieber group, a t-butyl Sieber group, and/or adialkoxybenzyl group. The linker may further contain one or moresubstituents selected from alkyl (such as C₁₋₆) or alkoxy (such asC₁₋₆), nitro, cyano, fluoro groups or groups with similar properties.Briefly, the linker can be cleaved by water-soluble phosphines and/orphosphine-based transition metal-containing catalysts. Other linkers andlinker cleavage mechanisms are known in the art. For example, linkerscomprising trityl groups, p-alkoxybenzyl ester groups, p-alkoxybenzylamide groups, tert-butyloxycarbonyl (Boc) groups, and acetal-basedgroups can be cleaved under acidic conditions by a proton-releasingcleavage agent such as an acid. A thioacetal or other sulfur-containinglinker can be cleaved using a thiophilic metals, such as nickel, silver,and/or mercury. The cleavage protecting groups can also be consideredfor the preparation of suitable linker molecules. Ester- and disulfidecontaining linkers can be cleaved under reductive conditions. Linkerscontaining triisopropyl silane (TIPS) or t-butyldimethyl silane (TBDMS)can be cleaved in the presence of F ions. Photocleavable linkers cleavedby a wavelength that does not affect other components of the reactionmixture include linkers comprising o-nitrobenzyl groups. Linkerscomprising benzyloxycarbonyl groups can be cleaved by Pd-basedcatalysts.

In some embodiments, the nucleotide precursor comprises a MNP labelattached to a polyphosphate moiety as described in, e.g., U.S. Pat. Nos.7,405,281 and 8,058,031. Briefly, the nucleotide precursor comprises anucleoside moiety and a chain of 3 or more phosphate groups where one ormore of the oxygen atoms are optionally substituted, e.g., with S. Thelabel may be attached to the a, (3, y or higher phosphate group (ifpresent) directly or via a linker. In some embodiments, the MNP label isattached to a phosphate group via a non-covalent linker as described,e.g., in U.S. Pat. No. 8,252,910. In some embodiments, the linker is ahydrocarbon selected from substituted or unsubstituted alkyl,substituted or unsubstituted heteroalkyl, substituted or unsubstitutedaryl, substituted or unsubstituted heteroaryl, substituted orunsubstituted cycloalkyl, and substituted or unsubstitutedheterocycloalkyl; see, e.g., U.S. Pat. No. 8,367,813. The linker mayalso comprise a nucleic acid strand; see, e.g., U.S. Pat. No. 9,464,107.

In embodiments in which the MNP is linked to a phosphate group, thenucleotide precursor may be incorporated into the nascent chain by thenucleic acid polymerase, which also cleaves and releases the detectableMNP. In some embodiments, the MNP is removed by cleaving the linker,e.g., as described in U.S. Pat. No. 9,587,275.

In some embodiments, the nucleotide precursors are non-extendable“terminator” nucleotides, i.e., the nucleotides that have a 3′-endblocked from addition of the next nucleotide by a blocking “terminator”group. The blocking groups are reversible terminators that can beremoved in order to continue the strand synthesis process as describedherein. Attaching removable blocking groups to nucleotide precursors isknown in the art. See, e.g., U.S. Pat. Nos. 7,541,444, 8,071,739 andcontinuations and improvements thereof. Briefly, the blocking group maycomprise an allyl group that can be cleaved by reacting in aqueoussolution with a metal-allyl complex in the presence of phosphine ornitrogen-phosphine ligands.

Detection Methods

Some embodiments herein are directed to detection methods that use adetection device and exploit the temperature-dependence of the magneticproperties of MNPs to detect the presence of molecules within a fluidicchannel (also referred to herein as a nanochannel, a nanofluidicchannel, and/or a microfluidic channel) of a detection device (exemplaryembodiments of which are described in the discussions of, for example,FIGS. 8A through 15 ).

In some embodiments, MNPs are coupled to molecules to be detected (e.g.,dNTPs in DNA sequencing applications) in any suitable way (e.g., asdescribed above). Using magnetic sensors (e.g., any of a variety ofembodiments of the magnetic sensors 105 described in further detailbelow), the detection device can then sense the presence and/or absenceof MNPs in one or more fluidic channels. By performing detection attemperatures both below and above what is referred to herein as acharacteristic temperature (e.g., the Curie temperature(s), the blockingtemperature(s), or any other temperature around which the magneticproperties of the MNP change) of the MNP(s) labeling the molecules to bedetected, the detection device can determine that a MNP is present whenit detects a magnetic field exceeding a threshold at a characteristictemperature below the applicable characteristic temperature but not at acharacteristic temperature above the applicable characteristictemperature (e.g., the Curie temperature(s) or the blockingtemperature(s)).

At various points in this document, it is assumed for convenience andsimplification of the explanation that the magnetic properties of a MNPchange abruptly around a characteristic temperature (e.g., the blockingtemperature, Curie temperature, etc.). It is to be understood, however,that the magnetic properties of a MNP might not, and need not, changeabruptly at the characteristic temperature. For example, at temperaturesin a range below but near the Curie temperature, the magnetization maygenerally decrease with increasing temperature (monotonically ornon-monotonically), eventually reaching a minimum value of about zero atthe Curie temperature. Accordingly, it will be appreciated that invarious embodiments disclosed herein, when detection below thecharacteristic temperature (e.g., Curie temperature or blockingtemperature) is performed, it may be desirable to perform detection at atemperature that is some number of degrees below the characteristictemperature. For example, it may be desirable, when performing detectionat a temperature below the Curie temperature, to set the temperature tosome percentage or fraction of the Curie temperature (e.g.,T_(m)=p×T_(c), where T_(m) is the temperature at which the detection isperformed and 0<p<1). As another example, it may be desirable to set thetemperature within a specified range below the Curie temperature, wherethere is a buffer between the top end of the specified range and theCurie temperature (e.g., T₁≤T_(m)≤T₂, where T_(m) is the temperature atwhich the detection is performed, T₁<<T_(c), and T₂<T_(c), and there isa buffer between T_(c) and T₂). The objective is to detect, based on asensed magnetic property, whether a MNP is in the vicinity of a magneticsensor, and those having ordinary skill in the art will understand howto select an appropriate temperature at which to perform detection basedon knowledge of the characteristic temperature, the magnetic propertiesof the selected MNP type at temperatures around the characteristictemperature, and the disclosures herein.

As a specific example of the use of MNPs for molecule detection, in DNAsequencing applications, molecules of each of the four types ofnucleotide precursors (A, T, C, and G) can be labeled by a MNP. Asindividual dNTPs are incorporated into target DNA strands present withinthe fluidic channel in the vicinities of magnetic sensors, the presence,at a particular magnetic sensor, of a sensed magnetic field associatedwith a MNP at a temperature below a characteristic temperature (e.g.,its Curie or blocking temperature) and the absence of a sensed magneticfield at a temperature above this characteristic temperature indicatesthat a nucleotide precursor labeled by that MNP has been incorporated ina DNA strand being sequenced and sensed by that particular magneticsensor. Conversely, when a particular magnetic sensor fails to detect amagnetic field associated with the MNP at a temperature below thecharacteristic temperature (e.g., the Curie temperature or blockingtemperature), it can be deduced that the nucleotide precursor labeled bythat MNP has not been incorporated into a DNA strand in the vicinity ofthe particular sensor.

Continuing with the example of DNA sequencing, there are at least twoways to perform DNA sequencing: (1) using a sequential binary methodwith one MNP type used to label all four nucleotide precursors, and (2)using multiple distinguishable MNP types, each labeling a different oneof the nucleotide precursors.

In a sequential binary method, the magnetically-labeled nucleotideprecursors (each labeled by the same type of MNP) are added one by oneto a detection device (e.g., to a fluidic channel of such a detectiondevice). A detection process follows the introduction of each nucleotideprecursor to detect whether that nucleotide precursor was incorporatedinto a DNA strand near each of one or more magnetic sensors. Followingthe addition of the MNP-labeled nucleotide precursor being tested, thetemperature is set to be within a first range that is either below orabove a characteristic (e.g., Curie or blocking) temperature of the MNPbeing used as a magnetic label, and the magnetic sensors are used todetect magnetic fields emanating from MNPs in their vicinities. Themagnetic sensors may detect magnetic fields by detecting, for example, aresistance, a voltage, a current, a frequency, a noise, and/or a changein resistance, voltage, current, frequency, and/or noise, and the outputof each magnetic sensor may indicate the magnitude of the fielddetected.

FIG. 2A illustrates an exemplary sequential binary method 500 suitablefor DNA sequencing in accordance with some embodiments. FIG. 2Aillustrates the exemplary method 500 assuming the Curie temperature isexploited, but it is to be appreciated that other characteristictemperatures, such as the blocking temperature, may be used instead. At502, the method begins. At 504, molecules of each the four nucleotideprecursors (A, T, C, and G) are all labeled by the same type of MNP. Thedifferent nucleotide precursors, each labeled by the same MNP type, arethen introduced one at a time into, for example, a fluidic channel of adetection device. Thus, at 506, a first nucleotide precursor to betested is selected. At 508, the selected (magnetically-labeled)nucleotide precursor is added to the fluidic channel of a detectiondevice. At 510, the temperature of the contents of the fluidic channelis set to a value below the Curie temperature of the MNP being used asthe magnetic label. The temperature may be set, for example, using atemperature control device (e.g., a heater) to heat the contents of thefluidic channel. Alternatively or in addition, the nucleotide precursormay be heated (or cooled) prior to being added to the fluidic channel.At 512, a selected magnetic sensor detects a first magnetic fieldmagnitude in its vicinity (e.g., presumed to be caused by MNPs withinthe fluidic channel). As explained above, the magnetic sensor(s) maysense the magnetic field emitted by one or more MNPs by detecting aresistance, a voltage, a current, a frequency, a noise, and/or a changein resistance, voltage, current, frequency, and/or noise. The sensingmay take place over a specified time period sufficient to reduce oreliminate transient effects (e.g., to provide an average). The sensedmagnetic field magnitude may be recorded.

At 514, the temperature of the contents of the fluidic channel is set toa value above the Curie temperature of the MNP being used as the label.The temperature may be set, for example, using a temperature controldevice (e.g., a heater) to heat the contents of the fluidic channel.Alternatively or in addition, the nucleotide precursor may be heated (orcooled) prior to being added to the fluidic channel. At 516, each of theselected one or more magnetic sensors detects a second magnetic fieldmagnitude in its vicinity (e.g., if present, presumed to be caused byMNPs within the fluidic channel). The sensed magnetic field magnitudemay be recorded. At 518, a binary (yes/no, I/O, etc.) determination maybe made based on the sensed magnetic fields at the two temperatures asto whether the magnetically-labeled nucleotide precursor being testedhas been incorporated into a DNA strand near each of the one or moremagnetic sensors. As shown in the exemplary method of FIG. 2A, if thefirst magnetic field magnitude is greater than a threshold (e.g., amagnetic field magnitude expected from a MNP in the magnetic sensor'svicinity) and the second magnetic field magnitude is less than thethreshold, then at 520 it is determined that the nucleotide precursorselected at 506 was incorporated into the target DNA strand(s)associated with (e.g., being sensed by) the magnetic sensor. Theidentity of either the nucleotide precursor itself or the complementarybase of the target DNA strand may be recorded, and the method ends at524.

If, however, it is determined at 518 that the first magnetic fieldmagnitude is not greater than the threshold or the second magnetic fieldmagnitude is not less than the threshold, then at 522 it is determinedwhether there are more nucleotide precursors to be tested during thesequencing cycle. If so, the MNPs may be cleaved from the DNAsub-strands, and the next nucleotide precursor may be introduced anddetected in a similar manner. In the exemplary embodiment of FIG. 2A,the method returns to 506, where another nucleotide precursor isselected, and the procedure described above is repeated. If, at 522, itis determined there are no more nucleotide precursors to be testedduring the current sequencing cycle, the method ends at 524.

Although FIG. 2A illustrates first setting the temperature of thecontents of the fluidic channel to a value below the Curie temperature,sensing the magnetic field, and then setting the temperature to a valueabove the Curie temperature and sensing the magnetic field, it is to beunderstood that the order of the temperature-setting steps may bereversed. For example, the temperature may first be set to a value abovethe Curie temperature for the first magnetic field magnitude sensingstep (514), and the contents of the fluidic channel may be cooled to avalue below the Curie temperature for the second magnetic fieldmagnitude sensing step (510). In other words, the second temperature iswithin a range that is above the Curie temperature if the firsttemperature was within a range below the Curie temperature, and thesecond temperature is within a range that is below the Curie temperatureif the first temperature was within a range above the Curie temperature.

Moreover, although FIG. 2A assumes that each of the nucleotideprecursors is labeled by the same type of MNP, it is not a requirementto use the same type of MNP for each of the nucleotide precursors. Forexample, it may be convenient to use the same type of MNP for each ofthe nucleotide precursors, but, alternatively, different nucleotideprecursors may be labeled by different types of MNP. In other words, twoor more of the nucleotide precursors may be labeled by the same type ofMNP, or two or more nucleotide precursors may be labeled by differenttypes of MNP.

The method 500 can be performed using one or more magnetic sensors. Itis to be appreciated that when more than one magnetic sensor is used,the decision at 518 can differ for different magnetic sensors. Forexample, in some types of SBS, a long strand of DNA is (or a pluralityof long strands of DNA from a single donor organism are) cut intosmaller, random-length segments prior to sequencing. All of thesesmaller strands, which are from the same donor, are randomizedsub-strands of the complete strand to be sequenced. For example, if thecomplete strand includes the sequence ATGGCTTAG, the smaller strandscould include, for example, distinct sub-strands (e.g., ATGG and TTAG)as well as, if a plurality of the longer strands are cut intosub-strands, sub-strands that partially or completely overlap othersub-strands (e.g., GGCTT and ATGGCT). All of the smaller, randomizedsub-strands may be sequenced at the same time, potentially after beingamplified. In such applications, it will be appreciated that because thesub-strands do not represent the same sub-sequences, it may be desirablefor each magnetic sensor to detect magnetic fields and/or changes inmagnetic fields caused by single MNPs because the sequencing of thesub-strands will not be coordinated (or synchronized) amongstsub-strands. For example, during a single sequencing cycle, a firstsub-strand may incorporate cytosine, a second sub-strand mightincorporate thymine, and a third sub-strand might incorporate adenine.In order to sequence multiple random segments of a larger nucleic acidstrand, it is desirable, in each sequencing cycle, to determine whetherand at which physical location(s) each dNTP type has been incorporated.Accordingly, when using the exemplary method 500 shown in FIG. 2A, thedecision at 518 may be “yes” for one magnetic sensor and “no” foranother. Thus, when sequencing randomized sub-strands of a nucleic acidsuch as DNA, it may be desirable to test all four nucleotide precursorsduring each sequencing cycle, even though for some of the magneticsensors the decision at 218 is “yes” for the first, second, or thirdtested nucleotide precursor.

Various other embodiments are directed to using multiple MNP types (forexample, MNP 1, 2, 3, and 4), each with, for example, a different T_(B)or T_(c) within a range of temperatures, from, for example, roomtemperature up to the temperatures used for different DNA sequencingchemistries (which can be on the order of 80-100 degrees Celsius).Focusing on the DNA example for illustration, each individual base (A,T, C, G) can be labeled by a different type of MNP (e.g., base A withMNP 1, base C with MNP 2, base G with MNP 3, and base T with MNP 4) byeither tagging each base separately and mixing them together orfunctionalizing each type of MNP differently so that it has an affinityfor a particular (e.g., its assigned) base. In a single chemistry run,all tagged (magnetically-labeled) bases may be introduced into amicrofluidic cell (e.g., the fluidic channel of the detection devicedescribed in detail below) in which DNA strands (e.g., fragments) to besequenced have been attached within the microfluidic cell (e.g., asdescribed in the discussion below of the detection device).

Accordingly, in some embodiments, instead of using a binary method withfour chemistry steps for each base read (sequencing cycle) as describedabove, either three or four different MNPs, each having, for example, adifferent Curie temperature, can be used as the magnetic labels, and allof them can be detected in a single chemistry step. For example, eachtype of molecule (e.g., in DNA sequencing applications, each dNTP type)can be labeled by a different MNP type, where each MNP type has adifferent Curie temperature and/or different temperature dependencearound the Curie temperature enabling it to be distinguished from allother MNPs being used as magnetic labels. For example, in a DNAsequencing application, A can be labeled by MNP1, T by MNP2, C by MNP3,and G either by MNP4 or left unlabeled, where the Curie temperatures ofMNP1, MNP2, MNP3, and (if used) MNP4 are all different enough that thethree or four types of MNPs can be distinguished by detecting whether,at a particular temperature, a magnetic field exceeding a threshold(which may be MNP-dependent or temperature-dependent, for example) isbeing emitted in the vicinity of a magnetic sensor. Then all three orfour magnetically-labeled nucleotide precursors can be introduced intothe fluidic channel at the same time, and changes in magnetic fields inthe vicinities of the magnetic sensors of the detection device can beused to identify which MNP (and, therefore, type of base), if any, hasbeen incorporated in the vicinity of each magnetic sensor. The targetDNA strands to be sequenced have already been attached to the detectiondevice with polymerase, which acts to incorporate nucleotide precursorsthat are complementary to those in the target strand.

Because the different MNP types coupled to different nucleotideprecursors have different Curie temperatures, and therefore switch frombeing ferromagnetic to being paramagnetic (or vice versa) at different,distinguishable temperatures, all four bases can be detected during asingle chemistry step. For example, in some embodiments, a firstmolecule type (e.g., adenine (A) in a DNA sequencing application) istagged by a first MNP type that has a first Curie temperature T₁, asecond molecule type (e.g., cytosine (C) in a DNA sequencingapplication) is tagged by a second MNP type that has a second Curietemperature a third molecule type (e.g., guanine (G) in a DNA sequencingapplication) is tagged by a third MNP type that has a third Curietemperature T_(c,3); and a fourth molecule type (e.g., thymine (T) in aDNA sequencing application) is tagged by a fourth MNP type that has afourth Curie temperature T_(c,4). The four molecule types can then bedistinguished by varying the temperature of the contents of the fluidicchannel and detecting, at each selected temperature, using magneticsensors, the magnetic field magnitude in the vicinity of each of thesensors. By comparing the magnetic field magnitudes at the varioustemperatures, it can be determined which, if any, of the four MNP typesis in the vicinity of each of the sensors.

For example, assume the Curie temperatures are in the relationshipT_(c,1)<T_(c,2)<T_(c,3)<T_(c,A). Assume further, for the sake ofexplanation, that the magnetizations of the MNPs are step-like abouttheir Curie temperatures, such that the first MNP type (“MNP1”) emits amagnetic field having a magnitude above a first threshold (“Th1”) attemperatures below T_(c,1) and below the first threshold at temperaturesabove T₁; the second MNP type (“MNP2”) emits a magnetic field having amagnitude above a second threshold (“Th2”) at temperatures below T_(c,2)and below the second threshold at temperatures above T_(c,2); the thirdMNP type (“MNP3”) emits a magnetic field having a magnitude above athird threshold (“Th3”) at temperatures below T_(c,3) and below thethird threshold at temperatures above T_(c,3); and the fourth MNP type(“MNP4”) emits a magnetic field having a magnitude above a fourththreshold (“Th4”) at temperatures below T_(c,4) and below the fourththreshold at temperatures above T_(c,4). (As explained above, themagnetization may change less abruptly about the Curie temperature thanthe step-like behavior assumed here, in which case “at temperaturesbelow [the Curie temperature]” may be interpreted as “at temperaturesbelow [the Curie temperature minus a suitable buffer].” Similarly, “attemperatures above [the Curie temperature]” may be interpreted as “attemperatures above [the Curie temperature plus a suitable buffer].”) Thethresholds may be in some kind of relationship (e.g., two or more of thethresholds can be the same, or all of the thresholds can be the same),or there may be no relationship between the thresholds (e.g., some orall of the thresholds can be different. In a DNA sequencing application,for example, the identity of the MNP, and therefore the identity of theincorporated nucleotide precursor (base incorporated in a target ssDNA)labeled by the MNP, can be determined using Table A below:

TABLE A Magnetic field magnitude emitted as a function of temperature(T) Base MNP Range 1: Range 2: Range 3: Range 4: (Pre- type T < T_(c, 1)T_(c, 1) < T < T_(c, 2) T_(c, 2) < T < T _(c, 3) T_(c, 3) < T < T_(c, 4)cursor) 4 >=Th4 >=Th4 >=Th4 >=Th4  T 3 >=Th3 >=Th3 >=Th3 <Th3 G2 >=Th2 >=Th2  <Th2 <Th2 C 1 >=Th1  <Th1  <Th1 <Th1 A

Thus, if, for example, the magnitude of the magnetic field detected by aparticular magnetic sensor is above a specified threshold, Th2, intemperature ranges 1 and 2, but below that threshold in ranges 3 and 4,it can be determined that MNP type 2 has been detected. In the exemplaryDNA sequencing application, therefore, the incorporated nucleotideprecursor is cytosine (C), and the identity of the last-paired base inthe DNA strand being sequenced is the complement of cytosine, which isguanine (G).

In embodiments in which each nucleotide precursor is labeled by adifferent MNP type, each different MNP type having a different Curietemperature, detection in the temperature range below the lowest Curietemperature of the MNPs (Range 1 in the table above) may be skippedbecause, as shown in the table above, all of the MNPs emit magneticfields having magnitudes exceeding their applicable thresholds.Alternatively, it may be desirable to perform detection in Range 1 todifferentiate between a sensor that has detected a MNP that transitionsbetween being ferromagnetic and paramagnetic and a sensor that is notnear any molecules being detected (or that does not have any moleculesto be detected in its vicinity). For example, in a DNA sequencingapplication, the results obtained in Range 1 can be used to determinewhether a particular magnetic sensor is in the vicinity of a DNA strandbeing sequenced. Because all of the MNPs emit magnetic fields in Range1, if a particular sensor does not detect a magnetic field having amagnitude exceeding one of the thresholds in Range 1, it can beconcluded that there is no DNA strand being sequenced in the regiondetectable by the particular sensor.

After some or all magnetic sensors have been read in each of thetemperature ranges, the MNPs may be cleaved from the incorporatedmagnetically-labeled nucleotide precursor using, for example, enzymaticor chemical cleavage, as is known in the art. The process can then berepeated for the next unpaired base in the strand being sequenced. Forat least DNA sequencing applications, this embodiment allows for asingle chemistry step per base read.

Thus, some embodiments herein that are suitable for DNA sequencingapplications are directed to a method of introducing all four nucleotideprecursors, each labeled by a different MNP type, into a detectiondevice fluidic channel (e.g., a flow cell array of magnetic sensors,described in more detail below) simultaneously or approximatelysimultaneously to enable a single template DNA base read. MNP typessuitable for such embodiments become paramagnetic at the temperaturesused for the chemistries that functionalize the nucleotide precursors(typically 80-100 degrees Celsius), and have different thermalstabilities so that they can be distinguished from each other. Asexplained above, the use of such MNP types allows the use of a singlechemistry cycle per base read, which can significantly increase thesequencing data collection throughput and decrease the amount of timeneeded to sequence a genome.

In some embodiments, the four nucleotide precursors are introduced intothe fluidic channel substantially simultaneously at a temperatureexceeding the highest blocking or Curie temperature of the MNP typesbeing used as magnetic labels. Under such conditions, all of the MNPslabeling nucleotide precursors are superparamagnetic or paramagnetic.This approach can mitigate (and, ideally, eliminate) magneticinteractions between the MNPs that might otherwise cause clumping orclustering of MNPs labeling different nucleotide precursors. In otherwords, as long as the magnetically-labeled nucleotide precursors areadded to the fluidic channel at a temperature above the highest blockingtemperature or Curie temperature, there will be little or no magneticinteraction between the MNPs when they are added to the fluidicchannel(s), which avoids clumping or clustering of multiple MNPs thatcould otherwise complicate detection of the individual bases and/orhamper the incorporation of the introduced nucleotide precursors withthe target DNA strands. The nucleotide precursors are given time to beincorporated into the target DNA strands (e.g., the polymeraseincorporates whichever of the nucleotide precursors is a match for thenext unpaired base of the DNA strand). The system may then be cooled toa lower temperature (e.g., room temperature) at which all of theintroduced MNPs are ferromagnetic to begin the measurement (sequencing)cycle, which could involve any number of magnetic detection schemes,including those mentioned above.

In some embodiments, the chemistry step to cleave and flush MNPs fromthe fluidic channel is also performed at a temperature above theblocking temperature or Curie temperature, also to prevent clumping andmagnetic interactions between MNPs being washed away.

Because the MNPs are ferromagnetic at the selected starting temperature(e.g., room temperature), any magnetic sensor configured to detectmagnetic fields at a site where a nucleotide precursor was incorporatedshould detect a MNP, but the identity of the MNP likely cannot bedetermined. By increasing the temperature of the system above the Curietemperature of one of the MNP types, however, that MNP type can be madeparamagnetic. Once paramagnetic, that MNP type will not generate amagnetic field, and it will no longer be detected by the magneticsensor. Therefore, subsequent measurements made after increasing thesystem temperature first above the Curie temperature of MNP1, then MNP1and 2, and finally MNP1, 2, and 3 will see more and more MNPs “drop out”and allow the sequencing system to distinguish which MNP, and thereforewhich base, was incorporated at a particular site in the array. Achemistry step can then be run to cleave and flush the MNPs, and theprocess can be repeated for the next unpaired base in the target DNAstrand. Here, the number of chemistry steps required is reduced to speedup the read process, which is primarily limited only by localheating/cooling times in the fluidic channel(s).

It is to be understood that, as explained previously, the temperaturesat which magnetic fields are detected need not be monotonicallyincreasing. For example, once the magnetically-labeled nucleotideprecursors have been added to the fluidic channel at a temperature abovethe highest Curie temperature of all of the MNPs being used, thetemperature can be cooled to be below only that highest Curietemperature. In general, the temperature can be varied in any selectedway to determine which, if any, MNP is being detected by a particularsensor.

FIG. 2B illustrates an exemplary method 550 suitable for DNA sequencingin which all four magnetically-labeled nucleotide precursors are addedto a fluidic channel of a detection device at the same (or substantiallythe same) time in accordance with some embodiments. FIG. 2B illustratesthe exemplary method 550 assuming the Curie temperature is exploited,but it is to be appreciated that other characteristic temperatures atwhich the MNP magnetic properties change, such as the blockingtemperature, may be used instead. At 552, the method begins. At 554,each nucleotide precursor is labeled by a different MNP type (e.g., A islabeled by MNP1, C by MNP2, G by MNP3, and T by MNP4, where MNP1, MNP2,MNP3, and MNP4 have distinguishable temperature-dependent thermalstabilities). For exemplary purposes, assume that the first MNP type(“MNP1”) emits a magnetic field having a magnitude above a firstthreshold (“Th1”) at temperatures below T_(c,1) and below the firstthreshold at temperatures above T₁; the second MNP type (“MNP2”) emits amagnetic field having a magnitude above a second threshold (“Th2”) attemperatures below T_(c,2) and below the second threshold attemperatures above T₂; the third MNP type (“MNP3”) emits a magneticfield having a magnitude above a third threshold (“Th3”) at temperaturesbelow T_(c,3) and below the third threshold at temperatures aboveT_(c,3); and the fourth MNP type (“MNP4”) emits a magnetic field havinga magnitude above a fourth threshold (“Th4”) at temperatures belowT_(c,4) and below the fourth threshold at temperatures above T_(c,4).(Again, as explained above, the magnetization may change less abruptlyabout the Curie temperature than the step-like behavior assumed here, inwhich case “at temperatures below [the Curie temperature]” may beinterpreted as “at temperatures below [the Curie temperature minus asuitable buffer].” Similarly, “at temperatures above [the Curietemperature]” may be interpreted as “at temperatures above [the Curietemperature plus a suitable buffer].”)

At 556, the temperature of the mixture of magnetically-labelednucleotide precursors (or the temperature of the fluidic channel of thedetection device) is set to a value above the highest Curie temperatureof the four MNP types. The temperature may be set, for example, using atemperature control device (e.g., a heater) to heat the contents of thefluidic channel. Alternatively or in addition, the nucleotide precursorsmay be heated (or cooled) prior to being added to the fluidic channel.With the assumptions set forth above, the highest Curie temperature isT_(c,4). At this temperature, all of the MNPs labeling the nucleotideprecursors are paramagnetic and are less likely to interact magneticallyand cause clumping or clustering. At 558, all of the nucleotideprecursors are added to the fluidic channel of the detection device(e.g., at the same time, at substantially the same time, or sequentiallybefore step 560 begins). After some period of time during which thenucleotide precursors are given time to be incorporated into target DNAstrands, at 560, the temperature of the fluidic channel is set to avalue below the lowest Curie temperature, T₁. (Again, as explainedabove, the choice to detect first at a temperature below the lowestCurie temperature is arbitrary and is not a requirement.) At 562, eachof a selected one or more magnetic sensors detects a first magneticfield magnitude in its vicinity (e.g., caused by MNPs within the fluidicchannel). As explained above, the magnetic sensor(s) may sense themagnetic field emitted by one or more MNPs by detecting a resistance, avoltage, a current, a frequency, a noise, and/or a change in resistance,voltage, current, frequency, and/or noise. The sensed first magneticfield magnitude may be recorded.

At 564, the temperature of the contents of the fluidic channel is set toa value between the lowest Curie temperature, T₁, and thesecond-to-lowest Curie temperature, T₂. The temperature may be set, forexample, using a temperature control device (e.g., a heater) to heat thecontents of the fluidic channel. At 566, each of the selected one ormore magnetic sensors detects a second magnetic field magnitude in itsvicinity (e.g., caused by MNPs within the fluidic channel). The sensedsecond magnetic field magnitude may be recorded.

At 568, the temperature of the fluidic channel is set to a value betweenthe second-to-lowest Curie temperature, T₂, and the second-to-highestCurie temperature, T_(c,3). The temperature may be set, for example,using a temperature control device (e.g., a heater) to heat the contentsof the fluidic channel. At 570, each of the selected one or moremagnetic sensors detects a third magnetic field magnitude in itsvicinity (e.g., caused by MNPs within the fluidic channel). The sensedthird magnetic field magnitude may be recorded.

At 572, the temperature of the fluidic channel is set to a value betweenthe second-to-highest Curie temperature, T_(c,3), and the highest Curietemperature, T_(c,4). The temperature may be set, for example, using atemperature control device (e.g., a heater) to heat the contents of thefluidic channel. At 574, each of the selected one or more magneticsensors detects a fourth magnetic field magnitude in its vicinity (e.g.,caused by MNPs within the fluidic channel). The sensed fourth magneticfield magnitude may be recorded.

At 576, the identity of the incorporated nucleotide precursor isdetermined based on an analysis of the first, second, third, and fourthmagnetic field magnitudes. The analysis may be conducted using a logictable similar to Table A shown above. Once the identity of theincorporated nucleotide precursor has been determined, it or theidentity of the complementary base may be recorded.

As explained above, it is to be understood that the order of certain ofthe steps shown in FIG. 2B can be modified. For example, although FIG.2B shows the first temperature at which magnetic fields are detected asbeing below the lowest Curie temperature, it should be appreciated thatthe first temperature could be in any of the ranges defined by the Curietemperatures of the MNPs. Specifically, it may be convenient to set thefirst temperature to a value between T_(c,3) and T_(c,4) so that thetemperature change between steps 556 and 560 is less than it would be ifthe first temperature were below T₁. Generally, temperature ranges maybe tested in any order. Accordingly, it is to be understood thepositions of steps 560 and 562, steps 564 and 566, steps 568 and 570,and steps 572 and 574 relative to each other may be modified (e.g.,steps 560 and 562 can be before or after any or all of steps 564 and566, steps 568 and 570, and steps 572 and 574).

Furthermore, it is to be understood that at step 556, the temperature ofthe mixture of magnetically-labeled nucleotide precursors (or thetemperature of the fluidic channel of the detection device) may be setto a value above the highest blocking temperature of the four MNP types(which may be less than the highest Curie temperature of the four MNPtypes). At this temperature, all of the MNPs labeling the nucleotideprecursors are superparamagnetic and are less likely to interactmagnetically and cause clumping or clustering.

After some or all magnetic sensors have been read in each of thetemperature ranges, the MNPs may be cleaved from the incorporatedmagnetically-labeled nucleotide precursors using, for example, enzymaticor chemical cleavage, as is known in the art. As explained above, thechemistry step to cleave and flush MNPs from the fluidic channel may beperformed at a temperature above the highest blocking temperature orCurie temperature, also to prevent clumping and magnetic interactionsbetween MNPs being washed away. A temperature control device (e.g., aheater) may be used to adjust the temperature of the contents of thefluidic channel prior to or during the washing step. The steps of themethod 550 can then be repeated for the next unpaired base in the strandbeing sequenced. For at least DNA sequencing applications, thisembodiment allows for a single chemistry step per base read.

As an example of the method 550, FIGS. 3A through 3E illustrate thesequencing operations using different MNP types for nucleic acidsequencing in accordance with some embodiments. FIG. 3A is a simplifiedillustration of two target DNA strands (templates) with polymerase boundto a fluidic channel of a sequencing device following incorporation ofthe MNP-labeled nucleotide precursors as described above. The labelednucleotides that are complementary to the next unpaired bases in thetarget DNA strands are incorporated into the DNA strands. In FIG. 3A, anadenine (A) nucleotide precursor labeled by MNP1 has been incorporatedin the DNA strand (fragment) at the site within the fluidic channel onthe left-hand side of FIG. 3A, and a cytosine (C) nucleotide precursorlabeled by MNP2 has been incorporated into the DNA strand (fragment) atthe site on the right-hand side of FIG. 3A.

The system is then cooled, to a first temperature (for example, roomtemperature) to begin the sequencing cycle. As shown in FIG. 3B,assuming that the first temperature (shown as 27 degrees Celsius) isbelow the lowest Curie temperature of all of the MNP types, the MNPslabeling the incorporated nucleotide precursors emit magnetic fields(labeled by left-pointing arrows) having magnitudes that can be detectedby magnetic sensors nearby.

After detection at the first temperature is complete, the system isheated to a second temperature that is above the lowest Curietemperature of the four Curie temperatures but below the remaining threeCurie temperatures. As shown in FIG. 3C, the MNP labeling the nucleotideprecursor on the left-hand side of the drawing (MNP1) becomesparamagnetic and no longer generates a magnetic field above a firstthreshold. Assuming that the MNP labels adenine (A), it can bedetermined that magnetic sensors that detected a magnetic fieldmagnitude above the first threshold at the first temperature but not atthe second temperature detected A. Therefore, the last-paired base ofthe template DNA strand is the complementary base, T.

After detection at the second temperature is complete, the system isheated to a third temperature that is above the second-lowest Curietemperature of the four Curie temperatures but below the second-highestCurie temperature of the four Curie temperatures. As shown in FIG. 3D,the MNP labeling the nucleotide precursor incorporated into the DNAstrand on the right-hand side of the drawing (MNP2) also becomesparamagnetic and no longer generates a magnetic field above a secondthreshold (which may be the same as or different from the firstthreshold used for the MNP types labeling other nucleotide precursors).Assuming the MNP labels cytosine (C), it can be determined that magneticsensors that detected a magnetic field magnitude above the secondthreshold at the second temperature but not at the third temperaturedetected C. Therefore, it can be concluded that the last-paired base ofthe template DNA strand is the complementary base, G.

After detection at the third temperature is complete, the system isheated to a fourth temperature that is above all but the highest Curietemperature of the four Curie temperatures. At this temperature, MNP3also becomes paramagnetic and no longer generates a magnetic field abovea third threshold (which may be the same as or different from the firstthreshold used for MNP1 and/or the second threshold used for MNP2).Assuming MNP3 labels guanine (G), it can be determined that magneticsensors that detected a magnetic field magnitude above the secondthreshold at the second temperature but not at the third temperaturedetected G. Therefore, it can be concluded that the last-paired base ofthe template DNA strand is the complementary base, C.

Following detection at the fourth temperature, the MNPs may be cleavedfrom the incorporated nucleotides and flushed out of the fluidicchannel(s) in a chemistry step, which may, but is not required to, beperformed at a temperature above the highest blocking temperature orCurie temperature to prevent clumping and magnetic interactions betweenMNPs being washed away. The process can then be repeated to identify thenext unpaired bases in the target DNA strands. The system temperaturecan be raised to a temperature greater than the highest Curie orblocking temperature of the four MNPs, new samples of the labelednucleotide precursors can be introduced, and the next sequencing cyclecan begin. In embodiments such as the one illustrated in FIGS. 3Athrough 3E, the number of chemistry steps used is reduced to speed upthe read process. The time required for each sequencing cycle isdependent on the heating/cooling time of the contents of the fluidicchannel.

Although FIGS. 3A through 3E illustrate an exemplary DNA sequencingembodiment in which a single chemistry step enables detection of allfour bases in a single step, as previously described, in otherembodiments, a similar process may be performed using one type of MNP(or fewer than four MNP types) and introducing and detecting fewer thanall bases at a time. For example, when a single MNP type is used, eachindividual base (nucleotide precursor) can be introduced and detectedsequentially, one at a time. In such embodiments, detection may beaccomplished in a binary manner, where the magnetic sensors detectwhether or not there is a magnetic field magnitude indicative of thepresence of the MNP type in the proximities of the magnetic sensors.This method may then be repeated for the remaining bases beforecleaving/washing away the MNPs and repeating the process for the nextunpaired base.

It is to be understood that it is not necessary to use four MNPs toperform detection using a single chemistry step. For example, in someDNA sequencing embodiments, one of the bases may be left unlabeled.Using the example above, and assuming that thymine (T) is leftunlabeled, the table becomes Table B below:

TABLE B Magnetic field magnitude emitted as a function of temperature(T) Base MNP Range 1: Range 2: Range 3: Range 4: (Pre- type T < T_(C, 1)T_(c, 1) < T < T_(c, 2) T_(c, 2) < T < T_(c, 3) T > T_(c, 3) cursor)None ~0 ~0 ~0 ~0 T 3 >=Th3 >=Th3 >=Th3  <Th3 G 2 >=Th2 >=Th2 <Th2 <Th2 C1 >=Th1  <Th1 <Th1 <Th1 ARelative to the example above, detection of the incorporation of A, C,and G is done as previously described, but the incorporation of T isdetected by detecting the absence of a magnetic field in the vicinity ofa magnetic sensor in each of the four temperature ranges. Optionally, atolerance can be used to create the detection range for the unlabeledbase to account for variations in stray magnetic fields in the vicinityof a magnetic sensor that is not near any MNP. Thus, if a magnetic fieldmagnitude larger than each of the thresholds is not detected in any ofthe temperature ranges, the absence of detectable magnetic field (ordetection of only a minimal magnetic field magnitude below what would beexpected to be emitted by a MNP in the temperature range) can beinterpreted as an indication that the last-incorporated nucleotideprecursor is thymine (and, therefore, that the last-paired base in theDNA strand being sequenced is the complement to thymine, which isadenine (A)).

In embodiments in which three nucleotide precursors are labeled bydifferent MNP types, each different MNP type having a different Curietemperature, and the fourth nucleotide precursor is left unlabeled,detection in the temperature range above the highest Curie temperatureof the MNPs (Range 4 in the table above) may be skipped because, asshown in the table above, all of the three MNP types fail to emitmagnetic fields having magnitudes exceeding their applicable thresholds,and the unlabeled nucleotide precursor also fails to emit a magneticfield. If Range 4 is skipped, it is possible to differentiate between amagnetic sensor that is not near any molecules being detected and asensor that has detected the unlabeled nucleotide precursor (e.g.,thymine in this example) during a particular sequencing cycle bycomparing the results over a number of sequencing cycles. For example,in a DNA sequencing application, if, after some number of sequencingcycles (e.g., a number exceeding the maximum expected number ofidentical bases in a row for the DNA sample being sequenced) and in allof the temperature ranges, a particular sensor never detects a magneticfield having a magnitude exceeding one of the thresholds, it can beconcluded that there is no DNA strand being sequenced in the region/areadetectable by the particular sensor. But if a particular sensorsometimes detects a magnetic field having a magnitude that exceeds oneof the thresholds in one or more of the temperature ranges (e.g., Ranges1, 2, and 3), it can be concluded that in sequencing cycles in which thesensor does not detect a magnetic field with a magnitude exceeding anyof the thresholds in any of the temperature ranges, thymine (T) wasincorporated during the corresponding sequencing cycle.

After some or all magnetic sensors have been read in each of thetemperature ranges, the MNPs may be cleaved from the incorporatedmagnetically-labeled nucleotide precursor using, for example, enzymaticor chemical cleavage, as is known in the art. The process can then berepeated for the next unpaired base in the strand being sequenced. Forat least DNA sequencing applications, this embodiment allows for asingle chemistry step per base read.

FIG. 4 illustrates an exemplary method 600 suitable for DNA sequencingin which three of the four nucleotide precursors are magneticallylabeled and added to a fluidic channel of a detection device at the same(or substantially the same) time as a fourth, unlabeled nucleotideprecursor in accordance with some embodiments. At 602, the methodbegins. At 604, each of three of the four nucleotide precursors islabeled by a different MNP type (e.g., A is labeled by MNP1, C by MNP2,and G by MNP3, where MNP1, MNP2, and MNP3 have distinguishable thermalstabilities). The fourth nucleotide precursor (e.g., T) is leftunlabeled. For exemplary purposes, assume that the first MNP type(“MNP1”) emits a magnetic field having a magnitude above a firstthreshold (“Th1”) at temperatures below T_(c,1) and below the firstthreshold at temperatures above T₁; the second MNP type (“MNP2”) emits amagnetic field having a magnitude above a second threshold (“Th2”) attemperatures below T_(c,2) and below the second threshold attemperatures above T₂; and the third MNP type (“MNP3”) emits a magneticfield having a magnitude above a third threshold (“Th3”) at temperaturesbelow T_(c,3) and below the third threshold at temperatures aboveT_(c,3).

At 606, the temperature of the mixture of nucleotide precursors (or thetemperature of the fluidic channel of the detection device) is set to avalue above the highest Curie temperature (or above the highest blockingtemperature). With the assumptions set forth above, the highest Curietemperature is T_(c,3). At this temperature, all of the MNPs labelingthe nucleotide precursors are paramagnetic (or superparamagnetic) andare less likely to interact magnetically and cause clumping orclustering. At 608, all of the nucleotide precursors are added to thefluidic channel of the detection device (e.g., at the same time, atsubstantially the same time, or sequentially before step 410 begins). At610, the temperature of the fluidic channel is set to a value below thelowest Curie temperature, T₁. At 612, each of a selected one or moremagnetic sensors detects a first magnetic field magnitude in itsvicinity (e.g., caused by MNPs within the fluidic channel). As explainedabove, the magnetic sensor(s) may sense the magnetic field emitted byone or more MNPs by detecting a resistance, a voltage, a current, afrequency, a noise, and/or a change in resistance, voltage, current,frequency, and/or noise. The sensed first magnetic field magnitude maybe recorded.

At 614, the temperature of the fluidic channel is set to a value betweenthe lowest Curie temperature, T₁, and the middle Curie temperature, T₂.At 616, each of the selected one or more magnetic sensors detects asecond magnetic field magnitude in its vicinity (e.g., caused by MNPswithin the fluidic channel). The sensed second magnetic field magnitudemay be recorded.

At 618, the temperature of the fluidic channel is set to a value betweenthe middle Curie temperature, T₂ and the highest Curie temperature,T_(c,3). At 620, each of the selected one or more magnetic sensorsdetects a third magnetic field magnitude in its vicinity (e.g., causedby MNPs within the fluidic channel). The sensed third magnetic fieldmagnitude may be recorded.

Optionally, at 622, the temperature of the fluidic channel is set to avalue above the highest Curie temperature, T_(c,3). Optionally, at 624,each of the selected one or more magnetic sensors detects a fourthmagnetic field magnitude in its vicinity, which should be near zerobecause all of the MNPs added to the fluidic channel should beparamagnetic at temperatures above the highest Curie temperature. Ifsteps 622 and 624 are performed, the sensed fourth magnetic fieldmagnitude may be recorded.

At 626, the identity of the incorporated nucleotide precursor isdetermined based on an analysis of the first, second, third, and (ifdetected) fourth magnetic field magnitudes. The analysis may beconducted using a logic table similar to Table B shown above. Once theidentity of the incorporated nucleotide precursor has been determined,it or the identity of the complementary base may be recorded.

It is to be understood that the order of certain of the steps shown inFIG. 4 can be modified. For example, although FIG. 4 shows the firsttemperature at which magnetic fields are detected as being below thelowest Curie temperature, it should be appreciated that the firsttemperature could be in any of the ranges defined by the Curietemperatures of the MNPs. Specifically, it may be convenient to set thefirst temperature to a value between T_(c,2) and T_(c,3) so that thetemperature change between steps 606 and 610 is less than it would be ifthe first temperature were below T₁. Generally, temperature ranges maybe tested in any order. Accordingly, it is to be understood thepositions of steps 610 and 612, steps 614 and 616, steps 618 and 620,and (if performed) steps 622 and 624 relative to each other may bemodified (e.g., steps 610 and 612 can be before or after any or all ofsteps 614 and 616, steps 618 and 620, and (if performed) steps 622 and624).

After some or all magnetic sensors have been read in each of thetemperature ranges, the MNPs may be cleaved from the incorporatedmagnetically-labeled nucleotide precursors using, for example, enzymaticor chemical cleavage, as is known in the art. The steps of the method600 can then be repeated for the next unpaired base in the strand beingsequenced. For at least DNA sequencing applications, this embodimentallows for a single chemistry step per base read.

Magnetic Sensors

The magnetic sensors used in embodiments described herein may be orcomprise, for example, magnetoresistive (MR) sensors that exploit MRprinciples. To understand how a MR device works, consider how anelectron in an electric current interacts with a thin film ferromagnetic(FM) layer. Quantum mechanics dictate that the probability is high thatan electron interacting with the FM layer will cause the electron spinto be oriented preferentially parallel or antiparallel to the directionof the magnet's moment for transmitted and reflected electronsrespectively, as shown in FIG. 5A. Electrons with spin parallel to themoment of the FM layer 204 preferentially pass through the FM layer 204(spin 210), whereas those with spin antiparallel preferentially arereflected back (spin 208). Due to this phenomenon, the interface betweena nonmagnetic (NM) layer 202 (assumed for purposes of this explanationto be a metal layer) and a FM layer 204 acts as a spin filter that canact to spin polarize (i.e., make one spin direction more preferential)an incoming electric current.

For a device with two FM layers 224 and 228 separated by a nonmagneticmetal layer 226 (spacer layer) as shown in FIGS. 5B and 5C, an incomingelectric current spin polarized by the first FM layer (FM1) 224interacts differently with the second FM layer (FM2) 228, depending onthe orientation of that layer's magnetic moment. If the moments of bothFM layers 224 and 228 are parallel to one another (FIG. 5B), then manyelectrons will pass through the device because many electrons in thecurrent will have their spin oriented with the moment of the second FM228 (spin 234). Few electrons will be reflected back (spin 232).

In the opposite case, where the moments of the two FM layers 224 and 228are oriented in an anti-parallel fashion (FIG. 5C), many electrons willbe blocked from passing through the second FM layer 228 (spin 236), andfar fewer electrons will traverse the device (spin 238). This means theamount of current passing through the device is dependent on theorientation of the two FM layers 224 and 228 with respect to oneanother. Because the resistance of the device is proportional to thecurrent, the resistance of the device is dependent on the orientation ofthe moments (i.e., the resistance is smaller when the moments areparallel than it is when they are antiparallel).

Whereas the above description presumes use of a nonmagnetic metal spacerlayer 226 separating the two FM layers 224 and 228 (a configuration alsoknown as a spin valve (SV) or giant magnetoresistance (GMR) device), aninsulating layer known as a tunneling barrier can alternatively be usedas the spacer layer separating the FM layers. In such implementations,the spacer layer may be made of a nitride or oxide-based material. Thesetypes of devices are called magnetic tunnel junctions (MTJs), and theyexhibit a similar resistance response (referred to as tunnelmagnetoresistance or TMR) because of spin polarized tunneling as opposedto spin filtering.

MR devices have been used in many applications, including magneticrecording, magnetic field sensing, and magnetic memory. In these cases,it is usually preferable to design the MR device to have one FM layer beeffectively “pinned” so that the direction in which its moment points instays fixed and is not easily altered by the application of a magneticfield. This is usually achieved by placing an antiferromagnetic (AFM)layer adjacent to the pinned layer and using an effect called exchangecoupling that provides strong unidirectional anisotropy for the FMlayer's moment. The second FM layer is left “free” to rotate under theimpulse of a magnetic field such that its moment rotates with respect tothe fixed orientation of the pinned FM layer so that the resistance ofthe device becomes a detector of the magnetic field direction oramplitude by effectively acting as a magnetic-field-to-voltagetransducer.

Magnetoresistance can be defined as

${{MR} = {R_{0} + {\Delta R{\sin^{2}\left( \frac{\theta}{2} \right)}}}},$

where R₀ is the resistance of the device when the moments are orientedin a parallel configuration, ΔR is the difference between resistance inparallel and antiparallel orientations, and θ is the angle between thetwo moments. For magnetic field sensing applications, a linear responseto the magnetic field is desired from the sensor. Considering theequation above, the sensor should ideally be designed and fabricated tohave the two FM layers oriented approximately 90° with respect to oneanother. This may be achieved by exchange biasing the pinned layer withan antiferromagnet and using a “hard bias” coating to rotate the freelayer approximately 90° away from the pinned layer. Further detail onthis design, as applied to embodiments related to sequencingapplications, will be given below.

FIG. 6 illustrates a portion of a magnetic sensor 105 in accordance withsome embodiments. The exemplary magnetic sensor 105 of FIG. 6 has abottom 108 and a top 109 and comprises three layers, e.g., twoferromagnetic layers 106A, 106B separated by a nonmagnetic spacer layer107. The nonmagnetic spacer layer 107 may be, for example, a metallicmaterial or combination of metallic materials, such as, for example,copper or silver, in which case the structure is called a spin valve(SV), or it may be an insulator such as, for example, alumina ormagnesium oxide, in which case the structure is referred to as amagnetic tunnel junction (MTJ). Suitable materials for use in theferromagnetic layers 106A, 106B include, for example, alloys of Co, Ni,and Fe (sometimes mixed with other elements). The example materialsdescribed above are merely exemplary and are not intended to belimiting. Materials suitable for use in MTJs are known to those havingordinary skill in the art.

In some embodiments, the magnetic sensor 105 is a thin-film device, andthe ferromagnetic layers 106A, 106B are engineered to have theirmagnetic moments oriented either substantially in the plane of the filmor substantially perpendicular to the plane of the film. Additionalmaterials may be deposited below and/or above the three layers 106A,106B, and 107 shown in FIG. 6 to serve purposes such as interfacesmoothing, texturing, and protection from processing used to pattern adetection device (described below), but the active region of themagnetic sensor 105 lies in the trilayer structure shown in FIG. 6 .Thus, a component that is in contact with a magnetic sensor 105 may bein contact with one of the three illustrated layers 106A, 106B, or 107,or it may be in contact with another part of the magnetic sensor 105that is not illustrated in FIG. 6 .

FIGS. 7A and 7B illustrate the resistance of MR sensors, which isproportional to 1-cos(θ), where θ is the angle between the moments ofthe two ferromagnetic layers 106A, 106B shown in FIG. 6 . To maximizethe signal generated by a magnetic field and provide a linear responseof the magnetic sensor 105 to an applied magnetic field, the magneticsensors 105 may be designed such that the moments of the twoferromagnetic layers 106A, 106B are oriented n/2 or 90 degrees withrespect to one another in the absence of a magnetic field. Thisorientation can be achieved by any number of methods that are known inthe art. As discussed above, one solution is to use an antiferromagnetto “pin” the magnetization direction of one of the ferromagnetic layers(either 106A or 106B, designated as “FM1”) through an effect calledexchange biasing and then coat the sensor with a bilayer that has aninsulating layer and permanent magnet. The insulating layer avoidselectrical shorting of the magnetic sensor 105, and the permanent magnetsupplies a “hard bias” magnetic field perpendicular to the pinneddirection of FM1 that will then rotate the second ferromagnet (either106B or 106A, designated as “FM2”) and produce the desiredconfiguration. Magnetic fields parallel to FM1 then rotate FM2 aboutthis 90 degree configuration, and the change in resistance results in avoltage signal that can be calibrated to measure the field acting uponthe magnetic sensor 105. In this manner, the magnetic sensor 105 acts asa magnetic-field-to-voltage transducer.

Note that although the example discussed immediately above described theuse of ferromagnets that have their moments oriented in the plane of thefilm at 90 degrees with respect to one another, a perpendicularconfiguration can alternatively be achieved by orienting the moment ofone of the ferromagnetic layers 106A, 106B substantially out of theplane of the film, which may be accomplished using what is referred toas perpendicular magnetic anisotropy (PMA).

Accordingly, the magnetic sensors can have any of a number ofconfigurations. For example, each of the magnetic sensors used inembodiments herein may be a thin-film device that uses the MR effect(e.g., it may be a MR sensor) to detect MNPs in a fluidic channel of adetection device (e.g., a DNA sequencing apparatus). Each magneticsensor may operate as a potentiometer with a resistance that varies asthe strength and/or direction of the sensed magnetic field changes. Eachmagnetic sensor may have dimensions of less than about 30 nm to detectmagnetic fields on the order of a few millitesla (mT).

It is to be understood that although much of this disclosure focuses onthe use of the resistance of magnetic sensors as a proxy for themagnetic field magnitude, the output provided by the magnetic sensorsmay be any suitable output, including, for example, a resistance, avoltage, a current, a frequency, a noise, and/or a change in resistance,voltage, current, frequency, and/or noise.

MR Sensor Array

FIGS. 8A through 8C illustrate an embodiment of a cross-point arrayarchitecture 300 that may be included in the detection device 100 inaccordance with some embodiments. For illustration, the magnetic sensors105 illustrated in FIGS. 8A through 8C comprise MTJ elements 308, but itis to be appreciated that other types of sensors (e.g., spin valvedevices) may be used. It is to be appreciated that although variousparticular MR sensor types were described above, the description is notintended to exclude other MR sensor types.

Referring to FIG. 8A, the cross-point array architecture 300 includestop wires 318 and bottom wires 320. As shown in the exemplary embodimentof FIG. 8A, the top wires 318 are oriented at substantially 90° anglesto the bottom wires 320 as shown. An example MTJ element 308 is situatedbetween a crossing of the array. The example MTJ element 308 includestwo or more FM layers separated by one or more non-magnetic layers 316(e.g., MgO). As shown, one of the FM layers is a free layer 310 thatwill rotate in the presence of a magnetic field, and another of the FMlayers is a pinned (or fixed) layer 314 that may be a single FM coupledto an AFM layer 312. Alternatively, a compound structure called asynthetic antiferromagnet (SAF) may be used. The SAF includes two FMlayers separated by a magnetic coupling layer (e.g., ruthenium), withone of the two FM layers coupled to an AFM layer. It is to be understoodthat although the example layer arrangement of MTJ element 308 shows ageneral structure with layers over or under other layers, interveninglayers not shown can be inserted.

To illustrate some of the features of the cross-point array architecture300, FIG. 8B shows a cross-section of the cross-point array architecture300 along the top wire 318 direction (indicated in FIG. 8A by thedash-dot line labeled “8B”), and FIG. 8C shows a cross-section of thecross-point array architecture 300 along the bottom wire 320 direction(indicated in FIG. 8A by the dashed line labeled “8C”). As shown, thesides of the MTJ elements 308 (which may be the magnetic sensors 105)are encapsulated by insulating material 336. Optionally, as shown inFIG. 8B, a hard bias magnetic material 338 may also be deposited betweenthe MTJ elements 308. If present, the hard bias magnetic material 338may be magnetized to point in a direction parallel to the direction ofthe top wire(s) 318. In embodiments including hard bias magneticmaterial 338, a thin layer of insulator 340 is also deposited on top ofthe hard bias magnetic material 338 to electrically insulate it from thetop wire(s) 318.

In some embodiments, the orientation of the free layer 310 moment is atan angle approximately 90° from the pinned layer 314 moment (as shown inthe left side panel of FIG. 13A, discussed further below), which can beachieved using one or more strategies. The first is by using a hard biasfield in which the hard bias magnetized along the direction of the topmagnet also applies a magnetic field across the MTJ elements 308 in thedirection of the top wire 318. Because the pinned layer 314 is fixedusing an AFM layer 312, its moment can be chosen to be perpendicular tothe hard bias field, but the free layer 310 will rotate to be roughlyparallel to the hard bias field.

A second way to achieve this orientation configuration is to pattern theMTJ elements 308 into rectangles or ellipses, where the long axis of theMTJ elements 308 is along the direction of the top wire(s) 318. Throughthe aspect ratio of these shapes, a shape anisotropy energy can betuned, which creates an axis along the length of the top wire(s) 318along which the free layer 310 magnetization will preferentially pointin the absence of an external magnetic field.

A third way to achieve this orientation configuration is by etching theFM layers 310, 314 along an axis to induce texturing (see, e.g., U.S.Pat. No. 7,382,586), which can also create uniaxial anisotropy so thatthe free layer 310 moment will point along the length of the top wire(s)318.

A fourth way to achieve this orientation configuration is to useperpendicular magnetic anisotropy to pull the free layer 310 out ofplane while keeping the pinned layer 314 in the plane of the film, orvice versa. The anisotropy of the free layer 310 is kept small enoughthat a small in-plane field can rotate the free layer 310 in plane,which is qualitatively similar to the other methods described above.There are other methods to achieve a 90° orientation between the freeand pinned layer moments in addition to those mentioned here, andachieving this orientation is not limited to these options.

Referring to FIG. 8C, the cross section shows the fluidic channels 115(e.g., nanofluidic or microfluidic channels), which may be, for example,trenches etched in an insulator. As shown, a small amount of insulator322 is left on the sidewalls of the magnetic sensors 105 (illustrated asMTJ elements 308) so that the MNPs do not electrically interact with themagnetic sensors 105. The portion of the insulator exposed to (andforming) the fluidic channel 115 may form the wall 117 to whichpolymerase molecules or molecules to be detected (e.g., nucleic acidsamples) may be attached for sequencing.

Detection Devices

FIGS. 9A, 9B, and 9C illustrate an exemplary detection device 100 inaccordance with some embodiments. The exemplary detection device 100,which is suitable for use with the methods described above, includes aplurality of magnetic sensors 105 arranged in an array 110 disposedadjacent to a fluidic channel 115. FIG. 9A is a top view of theapparatus, FIG. 9B is a cross-section view at the position indicated bythe dashed line labeled “9B” in FIG. 9A, and FIG. 9C is anothercross-section view at the position indicated by the dashed line labeled“9C” in FIG. 9A. Exemplary embodiments of the magnetic sensors 105 weredescribed above.

As shown in FIGS. 9A, 9B, and 9C, the exemplary detection device 100comprises a magnetic sensor array 110 that includes a plurality ofmagnetic sensors 105, with four magnetic sensors 105A, 105B, 105C, and105D shown in FIG. 9A. (For simplicity, this document refers generallyto the magnetic sensors by the reference number 105. Individual magneticsensors are given the reference number 105 followed by a letter.) It isto be understood that the detection device 100 may include more or fewerthan four magnetic sensors 105. The magnetic sensor array 110illustrated in the exemplary embodiment of FIG. 9A is a linear array.

In some embodiments, each of the plurality of magnetic sensors 105 iscoupled to at least one line 120 for reading an output from one or moreof the magnetic sensors 105. (For simplicity, this document refersgenerally to the lines by the reference number 120. Individual lines aregiven the reference number 120 followed by a letter.) The outputprovides an indication of magnetic field magnitude or a change inmagnetic field magnitude and may comprise, for example, a resistance, avoltage, a current, a frequency, a noise, and/or a change in resistance,voltage, current, frequency, and/or noise of the magnetic sensor 105. Inthe exemplary embodiment shown in FIG. 9A, each magnetic sensor 105 ofthe magnetic sensor array 110 is coupled to two lines 120. Specifically,the magnetic sensor 105A is coupled to the lines 120A and 120E, themagnetic sensor 105B is coupled to the lines 120B and 120E, the magneticsensor 105C is coupled to the lines 120C and 120E, and the magneticsensor 105D is coupled to the lines 120D and 120E. In the exemplaryembodiment, the lines 120A, 120B, 120C, and 120D reside under themagnetic sensors 105A, 105B, 105C, and 105D, respectively, and the line120E resides over the magnetic sensors 105. FIG. 9B shows the magneticsensor 105D in relation to the lines 120D and 120E.

The detection device 100 also includes a fluidic channel 115 that isadjacent to the magnetic sensor array 110. As its name suggests, thefluidic channel 115 is configured to hold fluids (e.g., liquids, gases,plasmas) when the detection device 100 is in use. The fluidic channel115 may by open (e.g., if its shape is rectangular, it may have threesides; if its shape is curved, it may have a shape that is a portion ofa cylinder; etc.) or closed (e.g., if its shape is cuboid, it may havesix sides; if its shape is curved, it may be cylindrical; etc.). Thefluidic channel 115 may include at least one movable piece (e.g., astopper, a flap, etc.) to allow fluid to enter into and/or exit thefluidic channel 115. The shape of the fluidic channel 115 may be regularor irregular. The fluidic channel 115 may include or may be coupled to apump that forces fluids into and/or out of the fluidic channel 115(e.g., through a membrane, opening, etc.). Alternatively, the fluidicchannel 115 may be a passive receptacle (e.g., it merely receives fluidsbut is not coupled to a device that injects or removes fluids).

As shown in FIG. 9B, the fluidic channel 115 has a wall 117 that isadjacent to the magnetic sensor array 110. The wall 117 may besubstantially vertical as illustrated in FIG. 9B. Alternatively, thewall 117 may be sloped at least in part (e.g., some or all of theinterior of the fluidic channel 115 may be curved (e.g., in the shape ofa portion or all of a cylinder) or non-vertical in part or in whole). Ingeneral, the fluidic channel 115 and wall 117 may have any shapes thatallow the magnetic sensors 105 to detect the presence of MNPs near orattached to the wall 117, within the fluidic channel 115.

As described above, when the detection device 100 is in use, themagnetic sensors 105 are able to detect magnetic fields and/or changesin magnetic fields caused by MNPs that are in the fluidic channel 115.In some embodiments, the magnetic sensors 105 are able to detectmagnetic field magnitudes caused by MNPs in the vicinity of the magneticsensors 105.

The wall 117 has properties and characteristics that protect themagnetic sensors 105 from whatever fluid is in the fluidic channel 115while still allowing the magnetic sensors 105 to detect magnetic fieldsand/or changes to magnetic fields in their vicinities due to MNPs thatare within the fluidic channel 115. For example, the material of thewall 117 (and potentially of the rest of the fluidic channel 115) may beor comprise an insulator. For example, in some embodiments, a surface ofthe wall 117 comprises polypropylene, gold, glass, and/or silicon. Inaddition, the thickness of the wall 117 may be selected so that themagnetic sensors 105 can detect magnetic fields caused by MNPs withinthe fluidic channel 115. In some embodiments, the wall 117 isapproximately 2 nm to approximately 20 nm thick. It is desirable for theMNPs coupled to molecules being detected to be close to the sensors 105but separated from them by enough insulator to electrically passivatethe magnetic sensors 105. The thickness of the wall 117 may be selectedto meet this objective. Those having ordinary skill in the art will beable to select a suitable material and a suitable thickness of the wall117.

FIG. 9C is a cross-section view of the detection device 100 along thedashed line labeled “9C” in FIG. 9A. Because the cross-section is takenat a point within the fluidic channel 115, the magnetic sensors 105 andlines 120 would not be visible and are, therefore, shown using dashedlines to illustrate their positions within the detection device 100. Asshown in FIG. 9C, in some embodiments, the wall 117 has a supportstructure 114 (or multiple support structures 114) configured to anchormolecules to be sensed (e.g., nucleic acid or molecules of a nucleicacid polymerase) to the wall 117 near the magnetic sensors 105. FIG. 9Cillustrates four individual support structures 114A, 114B, 114C, and114D, each of which corresponds to a magnetic sensor 105 (e.g., supportstructure 114A corresponds to magnetic sensor 105A, support structure114B corresponds to magnetic sensor 105B, etc.). The support structure114 (or support structures 114) of the wall 117 may include a cavity ora ridge to which molecules may be attached or anchored. Although FIG. 9Cshows individual support structures 114 corresponding to each of themagnetic sensors 105, the detection device 100 may have fewer or moresupport structures 114 than shown. For example, there may be moresupport structures 114 than magnetic sensors 105, such that eachmagnetic sensor 105 is near multiple support structures 114. As anotherexample, multiple magnetic sensors 105 may share a single supportstructure 114. As yet another example, multiple magnetic sensors 105 mayshare multiple support structures 114. In embodiments in which thedetection device 100 includes multiple support structures 114, thosesupport structures 114 may be the same as or similar to each other, orthey may be different from each other.

In some embodiments, it may be advantageous for each magnetic sensor 105to detect MNPs coupled to a single respective support structure 114. Forexample, in some types of SBS, a long strand of DNA is (or a pluralityof long strands of DNA from a single donor organism are) cut intosmaller, random-length segments prior to sequencing. All of thesesmaller strands, which are from the same donor, are randomizedsub-strands of the complete strand to be sequenced. For example, if thecomplete strand includes the sequence ATGGCTTAG, the smaller strandscould include, for example, distinct sub-strands (e.g., ATGG and TTAG)as well as, if a plurality of the longer strands are cut intosub-strands, sub-strands that partially or completely overlap othersub-strands (e.g., GGCTT and ATGGCT). All of the smaller, randomizedsub-strands may be sequenced at the same time, potentially after beingamplified. In such applications, it will be appreciated that because thesub-strands do not represent the same sub-sequences, it may be desirablefor each magnetic sensor 105 to detect magnetic fields and/or changes inmagnetic fields caused by single MNPs because the sequencing of thesub-strands will not be coordinated (or synchronized) amongstsub-strands. For example, during a single sequencing cycle, a firstsub-strand may incorporate cytosine, a second sub-strand mightincorporate thymine, and a third sub-strand might incorporate adenine.In order to sequence multiple random segments of a larger nucleic acidstrand, it is desirable, in each sequencing cycle, to determine whetherand at which physical location(s) each dNTP type has been incorporated.

To simplify the explanation, FIGS. 9A, 9B, and 9C illustrate anexemplary detection device 100 with a single fluidic channel 115 andonly four magnetic sensors 105A, 105B, 105C, 105D in the magnetic sensorarray 110. It is to be appreciated that the detection device 100 mayhave many more magnetic sensors 105 in the magnetic sensor array 110,and it may have either additional fluidic channels 115 or a moreintricate single fluidic channel 115 (e.g., with a different shape orwith interconnected channels). In general, any configuration of magneticsensors 105 and fluidic channel(s) 115 that allows the magnetic sensors105 to detect temperature changes caused by MNPs in the fluidicchannel(s) 115 may be used.

FIG. 9D is a block diagram showing an exemplary detection system 300 formolecule detection in accordance with some embodiments. As illustratedin FIG. 9D, the system 300 includes a detection device 100. As shown inthe exemplary embodiment of FIG. 9D, the detection device may comprisecontrol circuitry 130 coupled to the magnetic sensor array 110 via thelines 120. The control circuitry 130 may comprise any suitablecomponents, including, generally, suitable detection circuitry. Suchcontrol circuitry 130 may comprise hardware and/or software. The controlcircuitry 130 may include, for example, one or more of: a processorcapable of executing machine-executable instructions, anapplication-specific integrated circuit (ASIC), a controller, aprogrammable circuit (e.g., FPGA), etc.

As also shown in FIG. 9D, the detection system 300 may also include oneor more temperature control devices 140 (e.g., one or more heaters) and,optionally, one or more magnetic components 150. The magneticcomponent(s) 150 may comprise, for example, an electromagnet, adistributed coil, a solenoid, a permanent magnet, or a superconductingmagnet. If present, the magnetic component 150 may provide a static(e.g., constant in time or DC) magnetic field to align the magneticmoments of the MNPs in the fluidic channel 115 in substantially the samedirection. Although FIG. 9D illustrates the temperature controldevice(s) 140 and magnetic component(s) 150 as being separate from thedetection device 100, one or more of the temperature control device(s)140 and magnetic component(s) 150, if present, may be included in thedetection device 100, or one or both of the temperature controldevice(s) 140 and magnetic component(s) 150 may be separate from thedetection device 100.

In some embodiments, the system 300 includes one or more temperaturecontrol device(s) 140, which may comprise, for example, one or moreheating elements. For example, the system 300 may include a heatspreader, which may be coupled to the detection device 100. In someembodiments, the detection device 100 itself includes one or moreheating elements 142 coupled, for example, to its bottom surface 119.FIG. 10 is an exploded view of exemplary heating elements 142 suitablefor incorporation in or use with a detection device 100 in accordancewith some embodiments. The detection device 100 shown in FIG. 10includes or is coupled to a surface heater 142A that providessubstantially uniform heating across the bottom surface 119 of thedetection device 100. The detection device 100 shown in FIG. 10 alsoincludes linear heaters 142B at or near the edges of the bottom surface119 (see FIG. 12A), which may be used to remove a temperature gradientcaused by the surrounding environment being at a different (e.g.,cooler) temperature.

Alternatively or in addition, the detection device 100 may include anarray of heating elements 142, which may be useful if fine temperaturecontrol is desirable. FIG. 11 illustrates an array 144 of heatingelements 142 that may be coupled, for example, to the bottom surface 119of the detection device 100 in accordance with some embodiments. Toavoid obscuring the drawing, only a few of the heating elements 142 areshown with reference numbers.

As an example of a detection device 100 with a larger number of magneticsensors 105 in the magnetic sensor array 110, FIGS. 12A, 12B, 12C, and12D illustrate portions of an exemplary detection device 100 thatincludes several fluidic channels 115, one or more of which may be aseparate fluidic channel 115 in accordance with some embodiments, or theaggregation of which may be considered a single fluidic channel 115. Inthe embodiment of the detection device 100 shown in FIGS. 12A, 12B, 12C,and 12D, the plurality of magnetic sensors 105 of the magnetic sensorarray 110 is arranged in a rectangular grid pattern. Each of the lines120 identifies a row or a column of the magnetic sensor array 110. It isto be understood that FIGS. 12A, 12B, 12C, and 12D show only a portionof the detection device 100 to avoid obscuring the parts of thedetection device 100 being discussed. It is to be understood that thevarious illustrated components (e.g., lines 120, magnetic sensors 105,fluidic channels 115, etc.) might not be visible in a physicalinstantiation of the detection device 100 (e.g., some or all may becovered by protective material, such as an insulator). Moreover, asdiscussed herein, the detection device 100 may include other componentsnot illustrated in FIGS. 12A, 12B, 12C, and 12D.

FIG. 12A is a perspective view of the exemplary detection device 100 inaccordance with some embodiments. The exemplary detection device 100includes nine lines 120, labeled as 120A, 120B, 120C, 120D, 120E, 120F,120G, 120H, and 120I. It also includes five fluidic channels, labeled as115A, 115B, 115C, 115D, and 115E. As explained above, the fluidicchannels 115A, 115B, 115C, 115D, and 115E may be considered to beseparate fluidic channels 115 or a single fluidic channel 115. Thedetection device 100 also has a bottom surface 119.

FIG. 12B is a top view of the exemplary detection device 100 shown inFIG. 12A. The lines 120G, 120H, and 120I, which are not visible from thetop view, are shown using dashed lines to indicate their locations. Thelines 120A-120F are shown in solid lines but, as explained above, thelines 120A-120F might also not be visible in the top view (e.g., theymay be covered by protective material, such as an insulator).

FIG. 12C is a cross-sectional view of the detection device 100 along theline labeled “12C” in FIG. 12A. As shown, each of the lines 120A, 120B,120C, 120D, 120E, and 120F is in contact with the top of one of themagnetic sensors 105 along the cross-section (namely, line 120A is incontact with magnetic sensor 105A, line 120B is in contact with magneticsensor 105B, line 120C is in contact with magnetic sensor 105C, line120D is in contact with magnetic sensor 105D, line 120E is in contactwith magnetic sensor 105E, and line 120F is in contact with magneticsensor 105F). The line 120H is in contact with the bottom of each of themagnetic sensors 105A, 105B, 105C, 105D, 105E, and 105F. It is to beappreciated that although FIGS. 12A-12D illustrate the lines 120 incontact with the magnetic sensors 105, the lines 120 may, in general, becoupled to the magnetic sensors 105 (i.e., they may be directlyconnected, or there may be intervening components disposed between thelines 120 and the magnetic sensors 105).

Referring again to FIG. 12C, the magnetic sensors 105A and 105B areseparated by the fluidic channel 115A (unlabeled in FIG. 12C but shownin FIG. 12A). Similarly, the magnetic sensors 105B and 105C areseparated by the fluidic channel 115B, the magnetic sensors 105C and105D are separated by the fluidic channel 115C, the magnetic sensors105D and 105E are separated by the fluidic channel 115D, and themagnetic sensors 105E and 105F are separated by the fluidic channel115E. As discussed further below, either or both of the vertical wallsof each fluidic channel 115 may be the wall 117.

In some embodiments, each magnetic sensor 105 is assigned to a singlefluidic channel 115. For example, in the exemplary device illustrated inFIGS. 12A-12D, the magnetic sensors 105 coupled to the line 120A may beconfigured to sense the presence or absence of MNPs in the fluidicchannel 115A, the magnetic sensors 105 coupled to the line 120B may beconfigured to sense MNPs in the fluidic channel 115B, the magneticsensors 105 coupled to the line 120C may be configured to sense MNPs inthe fluidic channel 115C, the magnetic sensors 105 coupled to the line120D may be configured to sense MNPs in the fluidic channel 115D, andthe magnetic sensors 105 coupled to the line 120E may be configured tosense MNPs in the fluidic channel 115E.

In the exemplary embodiment illustrated in FIGS. 12A-12D, there are morecolumns of magnetic sensors 105 than there are fluidic channels 115(i.e., in the exemplary embodiment shown, there are six columnscorresponding to lines 120A-120F and only five fluidic channels115A-115E). In such embodiments, each wall of one fluidic channel 115may be the wall 117. In other words, a single fluidic channel 115 may besensed by twice as many magnetic sensors 105 as each of the otherfluidic channels 115. For example, in the exemplary embodiment of FIGS.12A-12D, any of the fluidic channels 115 may be sensed by two columns ofmagnetic sensors 105. For example, the fluidic channel 115B may besensed by the magnetic sensors 105 coupled to both lines 120B and 120C.In this example, the magnetic sensors 105 coupled to the line 120A wouldbe assigned to sense the contents of the fluidic channel 120A, themagnetic sensors 105 coupled to the line 120D would be assigned to sensethe contents of the fluidic channel 120C, the magnetic sensors 105coupled to the line 120E would be assigned to sense the contents of thefluidic channel 120D, and the magnetic sensors 105 coupled to the line120F would be assigned to sense the contents of the fluidic channel120E.

FIG. 12D is a cross-sectional view of the detection device 100 along theline labeled “12D” in FIG. 12A. As shown, the line 120E is in contactwith the top of each of the sensors 105G, 105E, and 105H along thecross-section. Each of the lines 120G, 120H, and 120I is in contact withthe bottom of one of the magnetic sensors 105 along the cross-section(namely, line 120G is in contact with magnetic sensor 105G, line 120H isin contact with magnetic sensor 105E, and line 120I is in contact withmagnetic sensor 105H).

As explained above, the lines 120 shown in FIG. 12D need not be indirect contact with the magnetic sensors 105; instead, they may beconnected through intervening components. For example, in someembodiments, such as shown in FIGS. 12E and 12F, the detection device100 includes a plurality of selector elements 111, each of which iscoupled to a respective one of the magnetic sensors 105, where each ofthe selector elements 111 exhibits thresholding behavior such that forvoltages above a particular value (V_(th)), the selector element 111 hashigh conductivity, and below that voltage the conductivity of theselector element 111 is effectively zero. The selector elements 111 maycomprise, for example, transistors, diodes, etc. As will be appreciatedby those having ordinary skill in the art, different schemes ofaddressing (selecting) the magnetic sensors 105 (individually or ingroups) can be used that ensure only the voltage dropped across theintended magnetic sensor(s) 105 is above V_(th). Accordingly, selectorelements 111 may be used reduce the chances of “sneak” currents thatcould transmit through neighboring elements and degrade the performanceof the detection device 100.

FIG. 12E illustrates an exemplary approach for selecting magneticsensors 105 in accordance with some embodiments. In the exemplaryembodiment shown in FIG. 12E, a respective selector element 111 (shownin the exemplary embodiment as a CMOS transistor) is coupled in serieswith the magnetic sensor 105. In this exemplary embodiment, three lines120A, 120B, and 120C allow an output from the magnetic sensor 105 to beobtained or sensed. Conceptually, the line 120A may be considered to bea read-out line, the line 120C may be considered to be a control line,and the line 120B may be considered to be either or both a read-out lineand a control line. Each magnetic sensor 105 of an array 110 may becoupled in series to a respective selector element 111. For more detailon configurations such as the exemplary one shown in FIG. 12E, see B. N.Engel, J. Akerman, B. Butcher, R. W. Dave, M. DeHerrera, M. Durlam, G.Grynkewich, J. Janesky, S. V. Pietambaram, N. D. Rizzo, J. M. Slaughter,K. Smith, J. J. Sun, and S. Tehrani, “A 4-Mb Toggle MRAM Based on aNovel Bit and Switching Method,” IEEE Transactions on Magnetics, Vol.41, 132 (2005).

FIG. 12F illustrates another exemplary magnetic sensor 105 selectionapproach in accordance with some embodiments. In the exemplaryembodiment shown in FIG. 12F, a selector element 111 (e.g., a diode or asimilar thresholding element, as is known in the art, such assemiconductor diodes, operational transconductance amplifiers (OTAs),vanadium oxide layers, capacitive threshold-logic gates, etc.) isdeposited “in-stack” together with each of the magnetic sensors 105,which are placed into a cross-point architecture. Although FIG. 12Fshows the in-stack selector elements 111 under the magnetic sensors 105,it is to be understood that the stacking of the in-stack selectorelements 111 and the magnetic sensors 105 may be reversed (i.e., thein-stack selector elements 111 may be over the magnetic sensors 105).Respective selector devices (e.g., CMOS transistors) may be used to turnon the individual lines 120A, 120B to address/access individual magneticsensors 105 in the detection device 100. The use of CMOS selecttransistors may be simple due to the prevalence of foundries availableto fabricate the front end (e.g., the nanofabrication to build the CMOStransistors and underlying circuitry), but the types of currents usedfor operation may use a cross-point design to eventually reach thedensities desired. Additional details on configurations suitable toselect magnetic sensors 105 (e.g., in cross-point arrays) may be foundin C. Chappert, A. Fert, and F. N. Van Daul, “The emergence of spinelectronics in data storage,” Nature Materials, Vol. 6, 813 (2007) andin J. Woo et al., “Selector-less RRAM with non-linearity of device forcross-point array applications,” Microelectronic Engineering 109 (2013)360-363.

In embodiments in which the magnetic sensors 105 are arranged in across-point array, entire columns or entire rows may be readsimultaneously to improve the accuracy of the detection.

As described herein, the exemplary detection device(s) 100 shown anddescribed herein (e.g., in reference to FIGS. 8A-12F) can be used withmethods using SBS protocols that use magnetically-labeled nucleotideprecursors. SBS involves binding of primer-hybridized template DNA,incorporation of a deoxynucleoside triphosphate (dNTP), and detection ofincorporated dNTP. The detection device 100 can be used to expose themagnetic sensors 105 to sequencing reagents in the fluidic channel(s)115 while protecting the magnetic sensors 105 using, for example, anelectrically-insulating material. As described herein, DNA synthesis maybe performed using polymerase molecules placed in the proximity of themagnetic sensors 105, which detect the presence of MNPs.

In particular, as described herein, either molecules of polymerase orfragments of single-strand nucleic acid may be attached to the sidewall(s) 117 of the fluidic channel(s) 115 in the proximity of one ormore of the magnetic sensors 105. Sequencing can then be performed byadding, to the fluidic channel(s) 115, a nucleic acid template (having aprimer binding site and an extendable primer) and magnetically-labelednucleotide precursors (at least some types of nucleotide precursorlabeled by a distinguishable MNP), and sequencing the nucleic acidtemplate by using the lines 120 to detect an output from the magneticsensors 105. The output may indicate which of the magnetically-labelednucleotide precursors has been incorporated into the extendable primer(e.g., if multiple nucleotide precursors, each labeled by a differentMNP type, are added to the fluidic channel(s) 115 at substantially thesame time), or it may indicate whether a particular magnetically-labelednucleotide precursor has been incorporated into the extendable primer(e.g., if different nucleotide precursors labeled by MNPs (which may bethe same type of MNP for each type of nucleotide precursor) are added tothe fluidic channel(s) 115 sequentially). For DNA sequencingspecifically, because adenine (A) pairs only with thymine (T), andcytosine (C) pairs only with guanine (G), detection of the MNPs enablesthe determination of which of the magnetically-labeled nucleotideprecursors has been incorporated. In particular, if the MNP labeling Ais detected, the recorded base is T (and vice versa), and if the MNPlabeling C is detected, the recorded base is G (and vice versa).

In some embodiments, target molecules to be detected (e.g., nucleic acidstrands to be sequenced) are attached to the walls 117 of the fluidicchannels 115 as shown in the left panel of FIG. 13A and may havepolymerase 410 introduced at this point. Individual bases with attachedMNPs may then be introduced into the fluidic channels 115. Theappropriate (complementary) base pair (i.e., for DNA sequencing,cytosine (C) with guanine (G) or adenine (A) with thymine (T)) will thenbe incorporated and can be detected. Assuming this process is done onebase pair at a time, sub-panel 402 (left) of FIG. 13A illustrates adetection method according to an embodiment in which the presence orabsence of the MNP, and therefore the base, can be determined using thevarious device embodiments of, for example, FIGS. 8A-12F. As shown insub-panel 402, polymerase 410 is bound to the wall 117 and is used tocapture induced DNA bases for detection.

Sequencing can occurs by applying a magnetic field (Happ) across the MTJelement 308 (an example of the magnetic sensor 105). The magnetic fieldmay be applied using an electromagnet, e.g., by placing the pole pieceson either side of the detection device), a distributed coil, a solenoidoriented perpendicular to the fluidic channel 115, etc. to generate themagnetic field in the direction of the pinned layer's moment 406. Themeans for generating the magnetic field may be mounted, for example, onthe bottom surface 119 of the detection device 100. As another example,the means for generating a magnetic field may be included in a systemthat includes the detection device 100. It is to be understood thatother suitable means of generating the magnetic field, such as, forexample, by using permanent magnets or super-conducting magnets, arepossible, are specifically contemplated herein, and are not excluded.

The applied magnetic field can achieve at least two objectives: (1) italigns the moments of all the MNPs in a common direction so that themeasured signals due to the presence of a MNP are similar, and (2) itrotates the free layer's moment 408 toward (or away from, depending onthe field orientation) the pinned layer's moment 406 and thus changesthe resistance of the magnetic sensor 105 from its equilibriumresistance.

The right-hand portion of FIG. 13A illustrates the pinned layer 314(labeled “fixed”) and free layer 310 as if viewing sub-panel 402 fromabove. The pinned layer 314 and free layer 310 are drawn offset fromeach other to illustrate their moments. The dashed line 424 shown in thefree layer 310 is the equilibrium direction of the free layer 310'smoment. In the absence of a MNP near the MTJ element 308 (or, moregenerally, the magnetic sensor 105), illustrated as case 418 (top) onthe right-hand side of FIG. 13A, the magnetic field can rotate themagnetic moment 408 of the free layer 310 into the direction of themagnetic moment 406 of the pinned layer 314 (depending on the details ofthe MTJ element 308/magnetic sensor 105 design). In the presence of aMNP near the MTJ element 308 (or, more generally, the magnetic sensor105), illustrated as case 420 (bottom) on the right-hand side of FIG.13A, fringing fields (Hparticle) will be created. These fringing fieldswill be in the same direction as the applied field and, therefore, canadd significantly to the applied field locally near the magnetic sensor105 (shown as a MTJ element 308). The magnetic moment 408 of the freelayer 310 will then rotate more substantially from its equilibriumposition (dashed line 424), as shown in case 420. Therefore, byconnecting the magnetic sensors 105 to detection electronics thatmeasure the resistance of the magnetic sensors 105 (or a proxy for theresistance, such as, for example, the voltage across the magneticsensors 105 for a given current), the presence or absence of a MNP canbe detected. The detection can be accomplished by either measuring theabsolute resistance of each magnetic sensor 105 (e.g., each MTJ element308) or by comparing the resistances to a reference cell or bit (e.g., amagnetic sensor 105 that is completely encapsulated such that it is notexposed to or affected by the field from a MNP).

FIG. 13B illustrates another embodiment in which the magnetic moments408 and 406 of, respectively, the free layer 310 and pinned layer 314are reversed in arrangement relative to FIG. 13A. The dashed line 434shown in the free layer 310 is the equilibrium direction of the freelayer 310's moment. As FIG. 13B illustrates, if the applied field Happis in the direction along the fluidic channel 115, the fringing fieldHparticle will be in an opposite direction to the applied field Happ.Thus, in the absence of a MNP near the MTJ element 308 (or, moregenerally, the magnetic sensor 105), illustrated as case 440 (top) onthe right-hand side of FIG. 13B, the magnetic field can rotate themagnetic moment 408 of the free layer 310 into the direction of themagnetic moment 406 of the pinned layer 314 (depending on the details ofthe MTJ element 308/magnetic sensor 105 design). In the presence of aMNP, however, the magnetic moments 408 and 406 will be closer to a90-degree alignment as shown in the bottom portion of the right-handside of FIG. 13B (case 450).

Method of Manufacturing Detection Device

In some embodiments, a detection device 100 is fabricated usingphotolithographic processes and thin film deposition. FIG. 14illustrates a method 850 of manufacturing the detection device 100, andFIG. 15 illustrates the results of each step of the fabrication process850 with a final panel showing polymerase bound to the wall 117proximate to a magnetic sensor 105 in accordance with some embodiments(e.g., when the detection device 100 is used for nucleic acidsequencing). At 852, the method begins. At 854, at least one line 120 isfabricated on a substrate, for example, by depositing one or more metallayers, using, for example, photolithography to pattern an array oflines and spaces in a polymer layer applied on top of the metal layers,using that polymer layer as a mask for etching the metal layers into anarray of lines, depositing an insulating dielectric material, strippingthe polymer layer and dielectric material over the lines, and performingchemical mechanical polishing to planarize the surface. At 856, themagnetic sensor array 110 is fabricated on the at least one line 120.Each magnetic sensor 105 of the magnetic sensor array 110 has a bottomportion 108 and a top portion 109. (See FIG. 6 .) The bottom portion 108is coupled to the at least one line 120. In some embodiments, the bottomportion 108 of each magnetic sensor 105 is in contact with the at leastone line 120.

At 858, dielectric material is deposited between the magnetic sensors105 of the magnetic sensor array 110. At 860, additional lines 120 arefabricated. Each of these additional lines 120 is coupled to the topportion 109 of at least one magnetic sensor 105 in the magnetic sensorarray 110. In some embodiments, the top portion 109 of each magneticsensor 105 is in contact with a line 120. In some embodiments, thebottom portion 108 of a magnetic sensor 105 is in contact with a firstline 120A, and the top portion 109 of the magnetic sensor 105 is incontact with a second line 120B. At 862, a portion of the dielectricmaterial adjacent to the magnetic sensors 105 is removed (e.g., bymilling, etching, or any other suitable removal process) to create thefluidic channel 115. At 864, the process 850 ends.

The embodiments disclosed herein offer several advantages. For example,as previously explained, an advantage of some embodiments is that theysimplify the introduction and incorporations of bases into themicrofluidic cell by forcing the magnetic nanoparticles used as tags tobecome paramagnetic when added to the fluidic channel of a detectiondevice, so that they do not interact with each other through magneticforces.

Another advantage of some embodiments is that they allow forsimultaneous tagging of all four nucleotide precursors in a manner thatallows them to be distinguished. This means a single chemistry step canbe used to read a single base in the target DNA strand with either threeor four subsequent measurements at, respectively, three or fourdifferent temperatures selected to exploit the temperature-dependence ofMNPs (e.g., that they are paramagnetic above the Curie temperature andferromagnetic below it). Because individual chemistry steps and take theorder of minutes, the disclosed embodiments can significantly speed upmolecule detection, such as DNA sequencing, without affecting the readerror rates.

As explained previously, although the description herein focuses on DNA,the various embodiments described can be applied to nucleic acidsequencing in general. Similarly, although SBS is used for illustrativepurposes in the description, the various embodiments are not so limitedto SBS sequencing protocols (e.g., dynamic sequencing could be usedinstead). The resulting array of magnetic sensors 105 (e.g., as shown inFIG. 6 ) can be used with a method that uses SBS protocols involving DNAbases (nucleotide precursors) labeled with MNPs. The array of magneticsensors coupled with an array of etched nanochannels (e.g., as shown inFIGS. 9 and 12A) may advantageously be used to expose individualmagnetic sensors 105 to sequencing reagents while protecting themagnetic sensors 105 with electrically insulating material. DNAsynthesis may be performed by polymerase molecules placed in theproximity of densely-packed magnetic field sensing elements (e.g.,magnetic sensors 105). SBS involves binding of primer-hybridizedtemplate DNA, insertion and incorporation of a deoxynucleosidetriphosphate (dNTP).

In particular, polymerase can be attached to the nanochannel side-wallsof a detection device 100 in the proximity of one or more magneticsensor elements within the array. For example, sequencing can beperformed by adding magnetic nanoparticles with DNA bases (four types ofnanoparticles, each group of nanoparticles containing only one kind oftethered base) into the nanofluidic or microfluidic channels, one typeof nanoparticles at a time. Since MNPs will only bind to polymerase withprimer-hybridized template DNA when the appropriate base pair isincorporated (i.e., cytosine (C) with guanine (G) or adenine (A) withthymine (T)), the detection of a magnetic particle will allow fordetermination of the base at the unterminated end of the template DNA.

In the foregoing description and in the accompanying drawings, specificterminology has been set forth to provide a thorough understanding ofthe disclosed embodiments. In some instances, the terminology ordrawings may imply specific details that are not required to practicethe invention.

To avoid obscuring the present disclosure unnecessarily, well-knowncomponents are shown in block diagram form and/or are not discussed indetail or, in some cases, at all.

Unless otherwise specifically defined herein, all terms are to be giventheir broadest possible interpretation, including meanings implied fromthe specification and drawings and meanings understood by those skilledin the art and/or as defined in dictionaries, treatises, etc. As setforth explicitly herein, some terms may not comport with their ordinaryor customary meanings.

As used in the specification and the appended claims, the singular forms“a,” “an” and “the” do not exclude plural referents unless otherwisespecified. Unless otherwise explicitly stated, articles such as “a” or“an” should generally be interpreted to include one or more describeditems. Accordingly, phrases such as “a device configured to” areintended to include one or more recited devices. Such one or morerecited devices can also be collectively configured to carry out thestated recitations. For example, “a processor configured to carry outrecitations A, B and C” can include a first processor configured tocarry out recitation A working in conjunction with a second processorconfigured to carry out recitations B and C.

The word “or” is to be interpreted as inclusive unless otherwisespecified. Thus, the phrase “A or B” is to be interpreted as meaning allof the following: “both A and B,” “A but not B,” and “B but not A.” Anyuse of “and/or” herein does not mean that the word “or” alone connotesexclusivity.

As used in the specification and the appended claims, phrases of theform “at least one of A, B, and C,” “at least one of A, B, or C,” “oneor more of A, B, or C,” and “one or more of A, B, and C” areinterchangeable, and each encompasses all of the following meanings: “Aonly,” “B only,” “C only,” “A and B but not C,” “A and C but not B,” “Band C but not A,” and “all of A, B, and C.”

To the extent that the terms “include(s),” “having,” “has,” “with,” andvariants thereof are used in the detailed description or the claims,such terms are intended to be inclusive in a manner similar to the term“comprising,” i.e., meaning “including but not limited to.” The terms“exemplary” and “embodiment” are used to express examples, notpreferences or requirements.

The terms “over,” “under,” “between,” and “on” are used herein refer toa relative position of one feature with respect to other features. Forexample, one feature disposed “over” or “under” another feature may bedirectly in contact with the other feature or may have interveningmaterial. Moreover, one feature disposed “between” two features may bedirectly in contact with the two features or may have one or moreintervening features or materials. In contrast, a first feature “on” asecond feature is in contact with that second feature.

Conditional language used herein, such as, among others, “can,” “could,”“might,” “may,” “e.g.,” and the like, unless specifically statedotherwise, or otherwise understood within the context as used, isgenerally intended to convey that certain embodiments include, whileother embodiments do not include, certain features, elements and/orsteps. Thus, such conditional language is not generally intended toimply that features, elements and/or steps are in any way required forone or more embodiments or that one or more embodiments necessarilyinclude logic for deciding, with or without other input or prompting,whether these features, elements and/or steps are included or are to beperformed in any particular embodiment.

The above detailed description has shown, described, and pointed outnovel features as applied to various embodiments, but it is to beunderstood that various omissions, substitutions, and changes in theform and details of the devices or algorithms illustrated can be madewithout departing from the spirit of the disclosure. As can berecognized, certain embodiments described herein can be embodied withina form that does not provide all of the features and benefits set forthherein, as some features can be used or practiced separately fromothers.

The drawings are not necessarily to scale, and the dimensions, shapes,and sizes of the features may differ substantially from how they aredepicted in the drawings.

Although specific embodiments have been disclosed, it will be evidentthat various modifications and changes may be made thereto withoutdeparting from the broader spirit and scope of the disclosure. Forexample, features or aspects of any of the embodiments may be applied,at least where practicable, in combination with any other of theembodiments or in place of counterpart features or aspects thereof.Accordingly, the specification and drawings are to be regarded in anillustrative rather than a restrictive sense.

We claim:
 1. A method of detecting molecules using a sequencing devicecomprising at least one fluidic channel and a plurality of magneticsensors configured to detect magnetic nanoparticles (MNPs) within the atleast one fluidic channel, the method comprising: adding, to the atleast one fluidic channel: (i) a first plurality of molecules to bedetected, at least some of the first plurality of molecules to bedetected being labeled by a first type of MNP, wherein the first type ofMNP has a first characteristic temperature such that, in a firsttemperature range, a magnitude of a magnetic field generated by thefirst type of MNP is greater than or equal to a first threshold, and, ina second temperature range, the magnitude of the magnetic fieldgenerated by the first type of MNP is less than the first threshold,wherein the first temperature range is lower than the second temperaturerange, and (ii) a second plurality of molecules to be detected, at leastsome of the second plurality of molecules to be detected being labeledby a second type of MNP, wherein the second type of MNP has a secondcharacteristic temperature, different from the first characteristictemperature, such that, in the first temperature range and in the secondtemperature range, a magnitude of a magnetic field generated by thesecond type of MNP is greater than or equal to a second threshold;setting a temperature within the at least one fluidic channel to bewithin the first temperature range; obtaining a first output from aselected one of the plurality of magnetic sensors while the temperatureof the at least one fluidic channel is within the first temperaturerange, the first output indicating a magnitude of a first detectedmagnetic field; setting the temperature within the at least one fluidicchannel to be within the second temperature range; obtaining a secondoutput from the selected one of the plurality of magnetic sensors whilethe temperature of the at least one fluidic channel is within the secondtemperature range, the second output indicating a magnitude of a seconddetected magnetic field; and determining, based at least in part on themagnitude of the first detected magnetic field and the magnitude of thesecond detected magnetic field, whether the first type of MNP or thesecond type of MNP has been detected by the selected one of theplurality of magnetic sensors, to detect a presence of either the firstor second plurality of molecules.
 2. The method of claim 1, wherein atleast one of the first output or the second output comprises one or moreof a resistance, a voltage, a current, a frequency, a noise, or a changein resistance, voltage, current, frequency, or noise.
 3. The method ofclaim 1, wherein the first threshold differs from the second threshold.4. The method of claim 1, wherein determining, based at least in part onthe magnitude of the first detected magnetic field and the magnitude ofthe second detected magnetic field, whether the first type of MNP or thesecond type of MNP has been detected by the selected one of theplurality of magnetic sensors comprises: in response to the magnitude ofthe first detected magnetic field being greater than or equal to thefirst threshold and the magnitude of the second detected magnetic fieldbeing less than the first threshold, determining that the first type ofMNP has been detected by the selected one of the plurality of magneticsensors, or in response to the magnitude of the first detected magneticfield being greater than or equal to the second threshold and themagnitude of the second detected magnetic field being greater than orequal to the second threshold, determining that the second type of MNPhas been detected by the selected one of the plurality of magneticsensors.
 5. The method of claim 1, wherein the first characteristictemperature is a first Curie temperature and the second characteristictemperature is a second Curie temperature.
 6. The method of claim 5,wherein the second Curie temperature is greater than the first Curietemperature, and further comprising: before adding, to the at least onefluidic channel, the first and second pluralities of molecules to bedetected, setting the temperature within the at least one fluidicchannel to a temperature value higher than both the first Curietemperature and the second Curie temperature, and wherein adding, to theat least one fluidic channel, the first and second pluralities ofmolecules to be detected occurs while the temperature within the atleast one fluidic channel is at the temperature value higher than thefirst Curie temperature and the second Curie temperature.
 7. The methodof claim 6, wherein the temperature value is a first temperature value,and further comprising: before adding, to the at least one fluidicchannel, the first and second pluralities of molecules to be detected,setting a temperature of a mixture of the first and second pluralitiesof molecules to be detected to a second temperature value higher thanboth the first Curie temperature and the second Curie temperature, thesecond temperature value being identical to or different from the firsttemperature value.
 8. The method of claim 1, wherein the firstcharacteristic temperature is a first blocking temperature and thesecond characteristic temperature is a second blocking temperature. 9.The method of claim 8, further comprising: before adding, to the atleast one fluidic channel, the first and second pluralities of moleculesto be detected, setting the temperature within the at least one fluidicchannel to a temperature value higher than both the first blockingtemperature and the second blocking temperature, and wherein adding, tothe at least one fluidic channel, the first and second pluralities ofmolecules to be detected occurs while the temperature within the atleast one fluidic channel is at the temperature value higher than boththe first blocking temperature and the second blocking temperature. 10.The method of claim 8, further comprising: before adding, to the atleast one fluidic channel, the first and second pluralities of moleculesto be detected, setting a temperature of a mixture of the first andsecond pluralities of molecules to be detected to a temperature valuehigher than both the first blocking temperature and the second blockingtemperature.
 11. The method of claim 1, wherein: the magnitude of themagnetic field generated by the first type of MNP is less than the firstthreshold in a third temperature range, the third temperature rangebeing higher than the second temperature range, and the magnitude of themagnetic field generated by the second type of MNP is less than thesecond threshold in the third temperature range, and further comprising:adding, to the at least one fluidic channel, a third plurality ofmolecules to be detected, at least some of the third plurality ofmolecules to be detected being labeled by a third type of MNP, whereinthe third type of MNP has a third characteristic temperature such that,in the first, second, and third temperature ranges, a magnitude of amagnetic field generated by the third type of MNP is greater than orequal to a third threshold; setting the temperature within the at leastone fluidic channel to be within the third temperature range; obtaininga third output from the selected one of the plurality of magneticsensors while the temperature of the at least one fluidic channel iswithin the third temperature range, the third output indicating amagnitude of a third detected magnetic field; and determining, based atleast in part on the magnitude of the third detected magnetic field,whether the third type of MNP has been detected by the selected one ofthe plurality of magnetic sensors.
 12. The method of claim 11, whereindetermining, based at least in part on the magnitude of the thirddetected magnetic field, whether the third type of MNP has been detectedby the selected one of the plurality of magnetic sensors comprises: inresponse to the magnitude of the first detected magnetic field beinggreater than or equal to the third threshold, and the magnitude of thesecond detected magnetic field being greater than or equal to the thirdthreshold, and the magnitude of the third detected magnetic field beinggreater than or equal to the third threshold, determining that the thirdtype of MNP has been detected by the selected one of the plurality ofmagnetic sensors.
 13. The method of claim 11, wherein the first, second,and third pluralities of molecules are added to the at least one fluidicchannel at a substantially same time.
 14. The method of claim 11,wherein at least two of the first, second, and third thresholds aredifferent.
 15. The method of claim 11, wherein the first characteristictemperature is a first Curie temperature, the second characteristictemperature is a second Curie temperature, and the third characteristictemperature is a third Curie temperature, wherein: the third Curietemperature is higher than the second Curie temperature, and the secondCurie temperature is higher than the first Curie temperature.
 16. Themethod of claim 15, further comprising: before adding, to the at leastone fluidic channel, the first, second, and third pluralities ofmolecules to be detected, setting the temperature within the at leastone fluidic channel to a temperature value higher than the first Curietemperature, the second Curie temperature, and the third Curietemperature, and wherein adding, to the at least one fluidic channel,the first, second, and third pluralities of molecules to be detectedoccurs while the temperature within the at least one fluidic channel isat the temperature value higher than the first Curie temperature, thesecond Curie temperature, and the third Curie temperature.
 17. Themethod of claim 11, wherein the first characteristic temperature is afirst blocking temperature, the second characteristic temperature is asecond blocking temperature, and the third characteristic temperature isa third blocking temperature: the third blocking temperature differsfrom the second blocking temperature, and the second blockingtemperature differs from the first blocking temperature.
 18. The methodof claim 11, wherein: the magnitude of the magnetic field generated bythe first type of MNP is less than the first threshold in a fourthtemperature range, the fourth temperature range being higher than thethird temperature range, the magnitude of the magnetic field generatedby the second type of MNP is less than the second threshold in thefourth temperature range, and the magnitude of the magnetic fieldgenerated by the third type of MNP is less than the third threshold inthe fourth temperature range, and further comprising: adding, to the atleast one fluidic channel, a fourth plurality of molecules to bedetected, at least some of the fourth plurality of molecules to bedetected being labeled by a fourth type of MNP, wherein the fourth typeof MNP has a fourth characteristic temperature such that, in the first,second, third, and fourth temperature ranges, a magnitude of a magneticfield generated by the fourth type of MNP is greater than or equal to afourth threshold; setting the temperature within the at least onefluidic channel to be within the fourth temperature range; obtaining afourth output from the selected one of the plurality of magnetic sensorswhile the temperature of the at least one fluidic channel is within thefourth temperature range, the fourth output indicating a magnitude of afourth detected magnetic field; and determining, based at least in parton the magnitude of the fourth detected magnetic field, whether thefourth type of MNP has been detected by the selected one of theplurality of magnetic sensors.
 19. The method of claim 18, whereindetermining, based at least in part on the magnitude of the fourthdetected magnetic field, whether the fourth type of MNP has beendetected by the selected one of the plurality of magnetic sensorscomprises: in response to the magnitude of the first detected magneticfield being greater than or equal to the fourth threshold, and themagnitude of the second detected magnetic field being greater than orequal to the fourth threshold, and the magnitude of the third detectedmagnetic field being greater than or equal to the fourth threshold, andthe magnitude of the fourth detected magnetic field being greater thanor equal to the fourth threshold, determining that the fourth type ofMNP has been detected by the selected one of the plurality of magneticsensors.
 20. The method of claim 18, wherein two or more of the first,second, third, and fourth thresholds are different.
 21. The method ofclaim 18, wherein the first, second, third, and fourth pluralities ofmolecules to be detected are added to the at least one fluidic channelat a substantially same time.
 22. The method of claim 18, wherein thefirst characteristic temperature is a first Curie temperature, thesecond characteristic temperature is a second Curie temperature, thethird characteristic temperature is a third Curie temperature, and thefourth characteristic temperature is a fourth Curie temperature,wherein: the fourth Curie temperature is higher than the third Curietemperature, the third Curie temperature is higher than the second Curietemperature, and the second Curie temperature is higher than the firstCurie temperature.
 23. The method of claim 22, further comprising:before adding, to the at least one fluidic channel, the first, second,third, and fourth pluralities of molecules to be detected, setting thetemperature within the at least one fluidic channel to a temperaturevalue higher than all of the first Curie temperature, the second Curietemperature, the third Curie temperature, and the fourth Curietemperature, and wherein adding, to the at least one fluidic channel,the first, second, third, and fourth pluralities of molecules to bedetected occurs while the temperature within the at least one fluidicchannel is at the temperature value higher than all of the first Curietemperature, the second Curie temperature, the third Curie temperature,and the fourth Curie temperature.
 24. The method of claim 18, whereinthe first characteristic temperature is a first blocking temperature,the second characteristic temperature is a second blocking temperature,the third characteristic temperature is a third blocking temperature,and the fourth characteristic temperature is a fourth blockingtemperature, and wherein: the fourth blocking temperature differs fromthe third blocking temperature, the third blocking temperature differsfrom the second blocking temperature, and the second blockingtemperature differs from the first blocking temperature.
 25. The methodof claim 11, wherein: the magnitude of the magnetic field generated bythe first type of MNP is less than the first threshold in a fourthtemperature range, the fourth temperature range being higher than thethird temperature range, the magnitude of the magnetic field generatedby the second type of MNP is less than the second threshold in thefourth temperature range, and the magnitude of the magnetic fieldgenerated by the third type of MNP is less than the third threshold inthe fourth temperature range, and further comprising: adding, to the atleast one fluidic channel, a fourth, unlabeled plurality of molecules tobe detected; setting the temperature within the at least one fluidicchannel to be within the fourth temperature range; obtaining a fourthoutput from the selected one of the plurality of magnetic sensors whilethe temperature of the at least one fluidic channel is within the fourthtemperature range, the fourth output indicating a magnitude of a fourthdetected magnetic field; and in response to the magnitude of the fourthdetected magnetic field being less than the first threshold, less thanthe second threshold, and less than the third threshold, determiningthat none of the first, second, or third type of MNP has been detectedby the selected one of the plurality of magnetic sensors.
 26. The methodof claim 11, wherein: the magnitude of the magnetic field generated bythe first type of MNP is less than the first threshold in a fourthtemperature range, the fourth temperature range being higher than thethird temperature range, the magnitude of the magnetic field generatedby the second type of MNP is less than the second threshold in thefourth temperature range, and the magnitude of the magnetic fieldgenerated by the third type of MNP is less than the third threshold inthe fourth temperature range, and further comprising: adding, to the atleast one fluidic channel, a fourth, unlabeled plurality of molecules tobe detected; setting the temperature within the at least one fluidicchannel to be within the fourth temperature range; obtaining a fourthoutput from the selected one of the plurality of magnetic sensors whilethe temperature of the at least one fluidic channel is within the fourthtemperature range, the fourth output indicating a magnitude of a fourthdetected magnetic field; and in response to the magnitude of the fourthdetected magnetic field being less than the first threshold, less thanthe second threshold, and less than the third threshold, determiningthat at least one of the fourth, unlabeled plurality of molecules hasbeen detected by the selected one of the plurality of magnetic sensors.